dilluns, 29 de febrer del 2016

SpineWave licenses Atlas Spine spacer system

Spinewave, Atlas Spine

Spine Wave said today it is licensing the True Position pivoting spacer system technology from Atlas Spine.

The center pivot point technology from the newly licensed True Position spacer allows for more easy and accurate position of interbody spacers, which Spine Wave said will be useful for surgeons implanting “crescent” type devices in a posterior-approach procedure.

“The True Position pivoting spacer System provides a unique interbody delivery solution for the surgeon focused on restoring a patient’s sagittal balance. We believe that the commercially available True Position device will be a great complement to our proprietary line of expandable spacers and we are equally excited about where our R&D effort with Atlas will take this important technology,” Spine Wave CEO Mark LoGuidice said in a press release.

Spine Wave said the true position pivoting spacer system is designed so it can be implanted using minimally invasive techniques. The system includes the True Position XL system designed to provide posterior implants with an implant “footprint”.

“As a company known for innovation and responsiveness, Spine Wave is the ideal partner to lead the True Position product franchise into its next stage of rapid market acceptance and innovation,” Atlas Spine CEO Douglass Watson said in a prepared statement.

Both companies said they will continue to collaborate on the development of future products using the True Position Pivoting Spacer System tech.

“Compared to other ‘crescent’ or ‘steerable’ devices I have used, I found this device to be significantly easier to accurately and reliably position in the optimal location. Going forward it will be an important part of my armamentarium,” Dr. Dom Coric of Charlotte, N.C.’s Carolina Neurosurgery & Spine Associates said in prepared remarks.

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EOS Imaging wins CE Mark for spineEOS

EOS ImagingEOS Imaging said today it won CE Mark approval in the European Union for its spineEOS 3D planning software for spinal surgery based on EOS bi-planar imaging.

The spineEOS 3D planning sotware is designed to allow surgeons to use 3D-imaging to create optimized treatment plans for improved sagittal alignment for pediatric patients with Adolescent Idiopathic Scoliosis, and adults with degenerative or deformative spine conditions.

“We are looking forward to highlighting our product offering at AAOS and share the value in the orthopaedic space of our EOS imaging platform and new EOSapps. These online 3D surgical planning solutions are a big step towards planning patient-specific procedures in 3D that are cost effective, and provide our company the exciting opportunity to offer full image-based services along key orthopedic care pathways,” CEO Marie Meynadier said in a press release.

The company’s newly released software provides treatment stimulation based on reference values and taking into account patient vertebrae shape and position in 3D. The company said the system is being used in clinical studies ongoing in San Diego, Calif. and Paris, France.

In December, EOS Imaging reported results from a a clinical study examining the association of sagittal balance measurements and risk of falling in elderly patients reported a correlation between the falling risk and postural balance measured using its sterEOS workstation.

In the 122-patient study, individuals received an EOS exam postural alignment parameters were measured with the sterEOS workstation postural analysis software. Results showed that specific parameters are associated with the risk of falling and can be used to improve individual falling-risk assessments.

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Regenerative firm Creative Medical launches cardio-focused AngioStem biz

Creative Medical HealthRegenerative biotech company Creative Medical Health said today it is launching a subsidiary biz, AngioStem, to commercialize its cardiovascular assets.

Assets on hand for the newly launched company include a therapy that uses autologous and allogeneic adult stem cells in combination with modulation of oxidative stress to treat heart failure in patients with cardiovascular disease, Creative Medical Health said.

“At Creative Medical Health, our mission is to identify promising technologies, add value by strengthening the science and intellectual property surrounding the technologies, and subsequently spin off new companies with specialized management teams. The development of a business strategy, the successful acquisition of independent funding to implement the strategy, and the recruitment of a management team to lead the strategy have positioned our cardiac stem cell technology to evolve from a promising technology into a functioning corporation,” Creative Medical Health CEO Timothy Warbington said in prepared remarks.

The company’s initial cardiovascular disease treatment patent also includes in-treatment assessment of oxidative stress, which Creative Medical Health said allows doctors the ability to personalize the treatment protocols.

“I look forward to working with the management team of AngioStem to bring stem cell technologies to patients who currently have no treatment options available. The promise of stem cell therapeutics offers the possibility of specifically utilizing cells of the body to accelerate healing. At AngioStem the aim is to utilize stem cells to generate new blood vessels, which may be applicable to conditions ranging from heart failure, to peripheral artery disease, to stroke,” Creative Medical Health founding board member Dr. Amit Patel said in a press release.

“Utilizing the clinical translational expertise of Dr. Amit Patel, our previous company Medistem was successful at taking a stem cell product from bench to bedside, resulting in a successful exit for our investors. We intend to replicate the previous success at AngioStem,” AngioStem CEO Thomas Ichim said in a prepared statement.

Creative Medical Health said ti owns a “portfolio of technologies” that include a patent for using autologous bone marrow stem cells to treat erectile dysfunction, which is currently in clinical trials.

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MassDevice.com +3 | The top 3 medtech stories for February 29, 2016

plus3-1x1

Say hello to MassDevice +3, a bite-sized view of the top three medtech stories of the day. This feature of MassDevice.com’s coverage highlights our 3 biggest and most influential stories from the day’s news to make sure you’re up to date on the headlines that continue to shape the medical device industry.

 

3. Report: Toshiba to sell entire medical equipment biz

MassDevice.com news

Toshiba reportedly plans to sell its entire medical equipment unit, Toshiba Medical Systems, rather than just a controlling stake, setting the stage for an aggressive bidding war that could drive the purchase price much higher than the $3.5 billion initial estimate.

A bidding war for a majority share in Toshiba Medical business was already heating up earlier this month among a slew of private equity players and rival corporations, as the Japanese industrial conglomerate sought outside investors. Also this month, Toshiba said it would either shut down or transfer all of its other healthcare businesses by the end of March. Read more


2. FDA mandates new study, ‘black box’ label for Bayer’s Essure

MassDevice.com news

The FDA said it would put a pair of measures in place for the controversial Essure permanent contraception device made by Bayer, mandating a new clinical study and new guidance on using the device.

Essure is a small metal coil that’s placed in the fallopian tubes via catheter. The FDA said last year that in the 13 years since Essure’s approval, the agency had received 5,093 complaints, including for pain or menstrual irregularities after using the device, and complaints of the device breaking. In addition to 5 fetal deaths, there were 4 reports of adult deaths for reasons such as infection and uterine perforation, the FDA said. Read more


1. Vascular Solutions, CEO Root beat criminal charges in off-label promotion case

MassDevice.com news

A federal jury acquitted Vascular Solutions and CEO Howard Root of charges that they ran an off-label promotion scheme for its now-discontinued Vari-Lase varicose vein treatment.

A grand jury in the U.S. District Court for Western Texas indicted Maple Grove, Minn.-based Vascular Solutions and Root in November 2014, alleging that they created a “Short Kit” version of the Vari-Lase device after an unidentified competitor won FDA clearance for a radiofrequency ablation device to treat perforator veins, because Vari-Lase was only cleared for treating superficial veins. Read more

The post MassDevice.com +3 | The top 3 medtech stories for February 29, 2016 appeared first on MassDevice.



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Endo tumbles on plans to shutter Astora biz

Endo, Astora Women's HealthEndo Health Solutions (NSDQ:ENDP) saw shares drop 20% today after announcing plans to close its Astora Women’s Health biz in March due to concerns over future product liability related to mesh implants, despite posting a solid earnings beat for Q4 and the full year 2015.

The company, along with other medical device makers, have been hit with series of lawsuits related to transvaginal meshes, intended to treat pelvic organ prolapse. Last July, Endo settled a batch of product liability lawsuits brought against subsidiary American Medical Systems Holdings over its pelvic mesh implants.

Last October the company agreed to put some 20,000 of the lawsuits to rest, saying it would increase the amount of money it had set aside to cover the claims from $1.2 billion to approximately $1.6 billion. In April 2014, Endo announced it reached agreements to settle up to approximately 21,700 additional mesh claims with separate plaintiffs’ law firms. In June 2013, it settled an undisclosed number of cases for $54.5 million.

The FDA, prompted by a significant increase in complaints about a type of surgical mesh used to treat pelvic organ prolapse in women, put the products under its most stringent level of review, Class III, in January.

Endo said it sought to divest itself of the Astora Women’s Health unit last year, but did not manage to sell the biz, and will now being winding down the business with a closure targeted at March 31.

“In 2015, the Company divested its AMS Men’s Health business and launched a strategic process for AMS Women’s Health – now Astora Women’s Health. While that process resulted in formal bids for Astora, Endo determined in the 1st quarter 2016 that it will wind down Astora business operations in order to reduce the potential for product liability related to future mesh implants. Endo will conduct a wind down process and work efficiently to support physicians in transitioning to alternative products. The company will cease business operations for Astora by March 31, 2016,” the company wrote in an SEC filing for its yearly earnings release.

Endo reported losses of $118.5 million, or 53¢ per share, on sales of $1.07 billion for the 3 months ended December 31. That amounts to a 121% growth in losses as sales stepped up 62% compared with the same period last year.

Adjusted to exclude 1-time items, earnings per share were $1.36, a solid 9¢ above the $1.27 analysts on Wall Street were looking for in the quarter.

For the full year, Endo reported losses of $1.5 billion, or $7.59 per share, on sales of $3.3 billion for the 12 months ended December 31. The company saw losses grow over 200% as sales only grew 37.3% compared with the last business year.

Adjusted to exclude 1-time items, earnings per share were $4.87, a solid 29¢ higher than analysts on the Street were expecting.

Despite beating the street in revenue and profits, the company has seen shares drop 20.7% as of 2:36 p.m. EST to trade at $42.00.

“Endo delivered solid financial results this quarter and was further strengthened by our first full quarter of revenues from the acquisition of Par Pharmaceutical Holdings, Inc. As we enter 2016, we believe our business is diversified and positioned for double-digit underlying growth over the mid- to long-term. Moving forward, we are focused on operational execution – especially on the integration of Par and on supporting growth for priority branded products such as Xiaflex and Belbuca – and continuing to create value for Endo shareholders,” CEO Rajiv De Silva said in an SEC filing.

News of the shuttering comes only days after the FDA scheduled a panel date to discuss the premarket approval submission from Astora Women’s Health for its Topas incontinence device. The company and federal watchdog were slated to meet in late February to consider the company’s sling mesh device.

The Topas is designed to be implanted around the puborectalis muscle for treating women with fecal incontinence who’ve failed more conservative therapies.

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Stentys touts data from head-to-head stent trial against MDT’s Resolute

StentysStentys SA (EPA:STNT) today touted the results of its Apposition IV trial comparing the company’s Stentys self-apposing sirolimus-eluting coronary stent to Medtronic‘s (NYSE:MDT) Resolute stent in patients with ST-segment elevation myocardial infarction.

Results from the study were published in the journal EuroIntervention this month.

Stentys calls its suite of Apposition stents the “world’s 1st and only self-apposing stent to treat acute myocardial infarction,” with a shape and size that adapts to “fit snugly” into blood vessels to prevent gaps that can lead to blood clots.

Data from the study indicated that Stentys-stent treated patients demonstrated statistically better stent apposition than those in the balloon-expandable Resolute group at 4 months, with a greater percentage of stents fully covered, the company said. The Stentys SES group showed no reduction in artery lumen diameter with near perfect strut coverage at 9 months, Stentys said.

“The Self-Apposing Sirolimus-eluting stent, which is now commercialized with its new delivery catheter under the brand Xposition S, is the only stent that can guarantee complete and continuous apposition even when treating heart attack patients. We believe this publication will reinforce the adoption of our technology among cardiologists looking for the optimal stent solution for their patients,” CEO Gonzague Issenmann said in prepared remarks.

A total of 152 patients were included in the trial, which was randomized 3:2 to the Stentys stent cohort. The trial took place over 19 months at 12 sites in 5 countries.

“The absence of any reduction in minimum lumen diameter combined with a very high rate of strut coverage is a good indicator of long-term safety for the Stentys SES. Another interesting finding is the augmented lumen size in the Stentys arm: with the addition of sirolimus elution, this benefit is extended to four and nine months,” study authors wrote.

The trial was originally launched in June 2012, when Stentys announced the trial pitting its Apposition stents against Medtronic’s Resolute.

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FDA approves InVivo neuro-spinal scaffold trial amendment

InVivo TherapeuticsInVivo Therapeutics (NSDQ:NVIV) said today the FDA approved a protocol amendment for its Inspire study examining the benefit of its Neuro-Spinal Scaffold for treating patients with complete thoracic AIS A spinal cord injuries, establishing objective performance criterion for the trial.

The newly set OPC for the trial is defined as 25% more of the patients in the study demonstrating an improvement of at least one ASIA Impairment Scale grade at 6 months after implantation, the Cambridge, Mass.-based company said. An OPC is a measure used in clincal studies designed to demonstrate safety and benefit to support a Humanitarian Device Exemption.

“The approval of this amendment, which includes the OPC, is one of the most important regulatory milestones the company has reached to date. The OPC provides additional clarity regarding our path to commercialization. We have made tremendous progress with the FDA over the past year in the design of The Inspire Study, and it is very rewarding to complete the design of a study that has the potential to change the standard of care for acute spinal cord injury patients,” CEO Mark Perrin said in a press release.

The Inspire study is slated to enroll 20 patients with complete AIS A spinal cord injuries, and will require 5 patients enrolled in the trial to convert to another AIS grade by 6-months to reach the OPC.

InVivo said that HDE approval is not guaranteed even if the OPC is met, and the device may be approved even if the OPC is not met, depending on if safety and a probable benefit are supported by a review of clincal endpoints and preclinical results.

Last week, InVivo saw shares rise as it announced the enrollment of the 6th patient in its Inspire pivotal clinical trial. The patient, who’s being treated at the Barnes-Jewish Hospital at Washington University Medical Center in St. Louis, Mo., was implanted with the InVivo device about 10 hours after a traumatic spinal injury, the company said.

Last month, InVivo Therapeutics said it won FDA approval to shift the Inspire pilot trial of its spinal scaffold to a pivotal probable benefit study. Earlier this month, the company added the University of California’s San Diego Medical Center as a site for the Inspire trial.

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Intuitive Surgical touts less complications in robot-assisted hysterectomy study

Intuitive SurgicalIntuitive Surgical (NSDQ:ISRG) today said that results from a study evaluating robotic-assisted hysterectomies were published in the International Journal of Gynecology and Obstetrics, indicating fewer complications in robot-assisted surgeries compared to conventional methods.

The study reported that individuals who underwent the surgery with the Sunnyvale, Calif.-based company’s da Vinci robotic system experienced fewer intraoperative complications than patients who underwent traditional abdominal or vaginal procedures, or those who had a laparoscopic procedure.

“It’s long been clear that minimally invasive hysterectomy can help reduce complications and speed recovery.  But past studies comparing open and minimally invasive approaches compared less experienced robotic-assisted surgeons with colleagues in other approaches. This study is designed to compare only the outcomes of similarly experienced surgeons, regardless of surgical approach, which provides a much more accurate picture of comparative effectiveness,” Dr. Peter Lim of Nevada’s Renown Regional Medical Center said in a press release. “Women in the robotic-assisted group had higher rates of obesity, adhesions and large uterus, suggesting that the robotic technology actually enables surgeons to perform surgery on more complex cases. This study gives women and the surgeons who care for them important insights to inform their decision making.”

Over 32,000 benign hysterectomy cases were analyzed in the study, which compared 30-day outcomes from robotic-assisted hysterectomies performed by high-volume surgeons with data from high-volume surgeons who performed abdominal, vaginal and laparoscopic hysterectomies, obtained from the Premier Perspective database. Included in the analysis were 2,300 robotic assisted surgeries, 9,745 abdominal, 8,121 vaginal and 11,952 laparoscopic surgeries, Intuitive Surgical reported.

“This study provides compelling and valuable evidence on the advantages of robotic-assisted benign hysterectomy. For women undergoing these procedures, the benefits of robotic-assisted surgery shown in this study carry real and tangible results for their recovery and return to everyday life,” chief medical officer Dr. Myriam Curet said in a prepared statement.

Last month, Intuitive Surgical announced the joint 510(k) clearance for it and Hill-Rom Holdings (NYSE:HRC) Trumpf Medical division’s Integrated Table Motion for its da Vinci Xi surgical system, which combines the robotic system and Trumpf’s TruSystem 7000dv advanced operating table.

The newly cleared Integrated table motion allows the operator to make a “comprehensive range of table adjustments” during surgical procedures, the company said. The table can be repositioned in real time while the robotic arms on the da Vinci system are docked, allowing the surgical system access to more regions of patients.

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TearLab to layoff 54 employees in restructuring

(NSDQ:TEAR) said today it is undertaking a strategic restructuring that will result in the loss of 54 employees as the company looks to tighten the bolts in pursuit of positive cash flow.

The San Diego, Calif.-based company said the reorganization of will cost approximately $300,000, but is expected to save the company $9.4 million compared to its full year 2015.

“We remain very excited about the momentum we built in 2015 and are well positioned for continued growth. Nevertheless, given the current market environment, we needed to take this difficult step now of restructuring the company to reduce spending and improve our operating efficiency. We believe that we now have the optimal sales force and office support staffing levels to successfully drive a new model that will allow us to continue to grow our device footprint and utilization. Our core focus going forward is to reach self-sustainability by driving increased adoption of our diagnostics platform,” CEO Seph Jensen said in prepared remarks.

Earlier this month, TearLab said it would be winding down its majority owned subsidiary OcuHub, expecting another $3.5 million reduction in operating expenses for the year as well.

The company said it will provide more info on the new operating model during its Q4 and full year 2015 conference call scheduled for March 8.

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Dentsply, Sirona Dental close $5.6B merger

Dentsply acquires SironaDentsply International (NSDQ:XRAY) and Sirona Dental Systems (NSDQ:SIRO) said today that they closed their $5.6 billion merger, after winning conditional approval last week from anti-trust regulators in the European Union.

Sirona agreed to extend licensing agreements between it and key suppliers, with York, Pa.-based Dentsply also agreeing to technical and legal safeguards for rival block suppliers and a fast-track arbitration process to resolve disputes. In January, the companies’ shareholders approved the proposed merger, which cleared the U.S. Federal Trade Commission’s waiting period last November.

The deal, announced in September, creates the world’s largest dental equipment maker. Sirona’s shareholders received 1.8142 XRAY shares for each SIRO share they owned; at roughly $98.06 apiece, that’s about a 0.7% discount on Sirona’s $99.31 closing price the day before the deal was announced.

The combined company, Dentsply Sirona, is slated to trade on the NASDAQ exchange under the XRAY symbol. At that point Dentsply shareholders will own 58% of the new entity, with Sirona shareholders owning the rest. Dentsply Sirona’s global headquarters will be in York, with international HQ at Sirona’a base in Salzburg, Austria.

“By combining Dentsply’s consumables platform with Sirona’s technology and equipment, the new company offers more products and integrated solutions than any other dental organization. Dentsply Sirona’s wide array of products for dental professionals and labs enable the treatment of general and specialty procedures including implantology, endodontics and orthodontics. With the broadest clinical education platform in the industry, the company is driving the adoption of new and approved technology and integrated solutions for more efficient workflows. Customer service and satisfaction will remain a key value to the new company and will be supported by the industry largest sales and service infrastructure comprised of direct sales and leading distributors,” the companies said in prepared remarks today. “The merger unites the 2 leading innovators in dental, each with over 100 years of experience. Combined, Dentsply Sirona will have largest and strongest R&D platform with over 600 experienced scientists and engineers to foster the development of better, safer and faster dental care.”

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Report: Toshiba to sell entire medical equipment biz

ToshibaToshiba (TYO:6502) reportedly plans to sell its entire medical equipment unit, Toshiba Medical Systems, rather than just a controlling stake, setting the stage for an aggressive bidding war that could drive the purchase price much higher than the $3.5 billion initial estimate.

A bidding war for a majority share in Toshiba Medical business was already heating up earlier this month among a slew of private equity players and rival corporations, as the Japanese industrial conglomerate sought outside investors. Also this month, Toshiba said it would either shut down or transfer all of its other healthcare businesses by the end of March.

Whatever its size, a deal would provide much-needed liquidity for Toshiba, which is facing mounting restructuring costs after a $1.3 billion accounting scandal. Citing “people familiar with the matter,” Reuters reported today that the rising costs prompted Toshiba’s management to pursue the sale of the entire business for as much as $5.75 billion (¥650 billion), much higher than the initial estimate of $3.5 billion to $4.4 billion (¥400 billion to ¥500 billion).

Private equity shop KKR and Toshiba rivals Fujifilm Holdings (TSE:4901) and Canon (NYSE:CAJ) are in the running, but Bain Capital and Carlyle group have dropped out of the bidding, the sources told Reuters. Other offers include joint bids by Konica Minolta (TYO:4902) and PE shop Permira. The deadline for bids is March 4.

Toshiba Medical Systems put up sales of $3.59 billion (¥405.6 billion) during fiscal 2015, which ended in March of that year.

($1 = ¥113.0)

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FDA mandates new study, ‘black box’ label for Bayer’s Essure

Bayer's Essure

The FDA today said it would put a pair of measures in place for the controversial Essure permanent contraception device made by Bayer (ETR:BAYN), mandating a new clinical study and new guidance on using the device.

Essure is a small metal coil that’s placed in the fallopian tubes via catheter. The FDA said last year that in the 13 years since Essure’s approval, the agency had received 5,093 complaints, including for pain or menstrual irregularities after using the device, and complaints of the device breaking. In addition to 5 fetal deaths, there were 4 reports of adult deaths for reasons such as infection and uterine perforation, the FDA said.

Earlier this month an analyst who examined the FDA’s adverse events website for cases involving the Essure device said the federal safety watchdog likely underestimated the number of fetal deaths linked to the implant.

Today the FDA said it would require Bayer to run a new trial designed to “determine heightened risks for particular women” and draft guidance including a boxed warning label explaining the potential for adverse events connected with Essure. Bayer must design and conduct the post-market surveillance study comparing Essure with laparoscopic tubal ligation, the FDA said, using measures such as rates of complications including unplanned pregnancy, pelvic pain and other symptoms, explantation surgery and an evaluation of the complications’ impact on quality of life.

“The actions we are taking today will encourage important conversations between women and their doctors to help patients make more informed decisions about whether or not Essure is right for them,” Dr. William Maisel, deputy director for science and chief scientist at the FDA’s Center for Devices & Radiological Health, said in prepared remarks. “They also reflect our recognition that more rigorous research is needed to better understand if certain women are at heightened risk of complications.”

The new draft guidance will also recommend a so-called “patient decision checklist” for physicians to discuss with patients “to better communicate risks and help to ensure an informed decision-making process,” the federal safety watchdog said. The agency is also recommending that patients implanted with Essure undergo a confirmation test 3 months after implantation to make sure that the scar tissue has enveloped the devices, ensuring that no eggs can pass through the fallopian tubes. The post-market study must also examine why some patients aren’t given the confirmation test at 3 months, the FDA said.

In a report issued before a September 2015 meeting of the FDA’s Obstetrics & Gynecology Devices advisory panel, the agency said it logged a nearly 1,400% spike in complaints filed over Essure in the last 3 years. During the hearing, Bayer’s director of global pharmacovigilance risk management, Dr. Andrea Machlitt, told the panel that the company received 17,000 adverse event reports, 15,000 from the U.S. The panel voted to recommend limited use of Essure until more is known about its safety.

In October 2015 a study found that women implanted with Essure were more than 10 times more likely to require post-procedure surgery than those who underwent laparoscopic sterilization.

A bill sponsored last year by Rep. Mike Fitzpatrick (R-Pa.) would ban U.S. sales of Essure altogether.

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Vascular Solutions, CEO Root beat criminal charges in off-label promotion case

Vascular SolutionsA federal jury last week acquitted Vascular Solutions (NSDQ:VASC) and CEO Howard Root of charges that they ran an off-label promotion scheme for its now-discontinued Vari-Lase varicose vein treatment.

A grand jury in the U.S. District Court for Western Texas indicted Maple Grove, Minn.-based Vascular Solutions and Root in November 2014, alleging that they created a “Short Kit” version of the Vari-Lase device after an unidentified competitor won FDA clearance for a radiofrequency ablation device to treat perforator veins, because Vari-Lase was only cleared for treating superficial veins.

Vascular Solutions, which agreed to a $520,000 settlement of a related civil suit in July 2014, contended that the Vari-Lase Short Kit brought in only $534,000 from 2007 to July 2014, when the company pulled it from the market. Root said Feb. 26 in prepared remarks that he and the company are “vindicated” by the verdict, which cannot be appealed, “but outraged by the obscene legal process we were forced to endure.”

“We greatly appreciate the jury’s complete rejection of the government’s false allegations. But to get to this result, we were subjected to 5 years of attacks which forced us to hire 10 separate law firms at a cost of over $25 million to defend against a criminal prosecution that clearly was never warranted by the facts. This case centered on just 1 version of just 1 of our more than 100 medical devices – a version that was FDA-cleared, made up only 0.1% of our sales, and, by the government’s own admission, never harmed a single patient. To say that this prosecution was wrong-headed and disproportionate would be the understatement of the year,” Root said.

“While this matter is now over for Vascular Solutions and me, an upcoming criminal trial remains scheduled for one of the company’s sales representatives on obstruction of justice charges because he refused to change his grand jury testimony to match what these prosecutors wanted to hear.  It should now be obvious that our sales rep’s indictment was merely a malicious retribution by misguided prosecutors, an action that needs to be corrected immediately.  And after his indictment is dismissed, if the U.S. Attorney in San Antonio still wants to prosecute someone for obstruction of justice in this case, in my opinion he wouldn’t even have to leave his own office to find the most suitable person to indict,” he added.

Root said that the U.S. Justice Dept. should review every off-label promotion case “to make sure their prosecutors’ theories comply with the law, not just their wishes.”

VASC shares closed up 9.9% on the news at $28.85 apiece Feb. 26.

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In brief: Latest version of ISO 13485 published

Emergo GroupBy Stewart Eisenhart, Emergo Group

The International Standards Organization has officially published the highly anticipated update to its ISO 13485 quality management system standard.

ISO 13485:2016 updates will impact several quality processes and procedures for medical device companies whose compliance to the standard is required for registrations in various markets worldwide.

Additional analysis of ISO 13485:2016 changes is available via Emergo’swhitepaper.

Stewart Eisenhart covers medical device regulatory affairs for Emergo Group.

The opinions expressed in this blog post are the author’s only and do not necessarily reflect those of MassDevice.com or its employees.

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divendres, 26 de febrer del 2016

They sold their company to Boston Scientific and then reacquired the technology years later – the unique story of NuCryo Vascular

Kevin Beedon, NuCryo Vascular

NuCryo Vascular GM      Kevin Beedon

Welcome to the Medsider interview series, a special new feature at MassDevice, which will appear regularly. All interviews are conducted by Scott Nelson, Founder of Medsider and Partnership Lead at Touch Surgery. We hope you enjoy them!

Because of diminishing margins, a lot of major medical device companies continue to add products to their sales bag in hopes of meeting top-line revenue goals. But successfully selling the entire bag can be challenging.

When the bag gets too big, a typical sales force will usually focus only on products that generate the most revenue. So what about the products that don’t product much revenue? Well, they’re sometimes just lost in the dust.

In the following interview with Kevin Beedon, General Manager of NuCryo Vascular, we learn how their team is taking advantage of this very scenario as they look to commercialize the newly redesigned PolarCath device.

The following conversation is based on an audio interview with Scott Nelson and Kevin Beedon. Scott is the Founder of Medsider and leads partnerships at Touch Surgery.

Scott Nelson:            Let’s start with NuCryo because it’s an an interesting story. And by the way, congrats on your recent 510(k) clearance. The cryo-catheter device that you’re commercializing has a storied history with the likes of Dr. James Joye, who initially founded CryoVascular Systems, the acquisition by Boston Scientific, and so on. Can you provide a high-level overview of the history, and then we’ll dig into the details later on in our conversation.

Kevin Beedon:          I do think it’s a great story and it’s a pretty unique opportunity because of the history of cryoplasty and the previous proven customer base that we’ve had. But back in the day, Boston Scientific acquired the PolarCath line from CryoVascular Systems, which was a startup formed and created by Dr. Joye. In its heyday, there was over $40 million in revenue from this product line, over 350 accounts, and approximately 900 to 1,000 physicians that had been trained on the product. But Boston Scientific went through a reorganization back in 2012. And it was their decision at the time to eliminate some products that they perceived to be costly too make, that weren’t within their core focus areas, had a small revenue stream compared to the larger coronary and CRM product lines that they offered. So at that time, they decided to stop manufacturing the product and it was deemphasized from the perspective of their sales force. So in 2014, the cryoplasty balloon, PolarCath, still had about $5.3 million in revenue and over 100 accounts using it, but sales were dwindling along with Boston Scientific’s inventory.

Dr. Joye and a few of the early investors in cryoplasty decided to create a company called Gemini NuCryo to buy back the rights from Boston Scientific with the intent to do some engineering modifications and bring it back to market. And that’s where we are in the present day. We did have an exclusive distribution deal last year with Vascular Solutions. But that was terminated in December of 2015 and we’re now moving forward with a direct sales force model for Gemini NuCryo.

Scott Nelson:            Certainly an interesting story, and to set the stage for those that are reading, this was a really successful product. In fact, I remember competing against the PolarCath device, and then it seemed like it just disappeared. There wasn’t a major recall. There wasn’t any data that was released that suggested it didn’t work. It just sort of, like I said, kind of disappeared. On that note, what’s your take on the reason for Boston Scientific deemphasizing it? It makes you wonder how often this really happens with large strategics like Boston Scientific, Medtronic, Stryker, etc.

Kevin Beedon:          I think that’s a great question, and obviously, I’m not going to speak on behalf of Boston Scientific. But I think back in the 2012 timeframe when these decisions were being made, post Boston’s acquisition of Guidant, there was a lot of change taking place in the industry. And so I believe they just made a decision that it was a smaller product line within the peripheral space and they decided to divest and stop manufacturing the product. But there never was a recall. In fact, in 2011 at TCT, there was very positive data to support cryoplasty, which was later published in 2012. It was called the COBRA study, which was a randomized prospective multicenter study comparing cryoplasty versus PTA in the post dilation of nitinol stents in the diabetic patient population. So it’s very, very positive data that a lot of physicians aren’t familiar with. In fact, a lot of physicians were also disappointed that the product went away. And so when we started reviving cryoplasty last year, physicians were surprised, but also very happy that they would have the opportunity to put PolarCath or cryoplasty back in their treatment algorithm for peripheral vascular disease.

Scott Nelson:            During my time at Covidien and Medtronic, there was a similar situation with one of our devices. It was relatively expensive to manufacture and sales were relatively low in comparison to other product franchises. So the decision was made to stop, not discontinue it per se, but really just stop selling it. And I know physicians weren’t very enthused about that decision. As I said earlier, you just wonder how often this really takes place with other companies. Regardless, it seems like a great opportunity for NuCryo.

Kevin Beedon:          I agree 100%. And I think what it comes down to is larger companies have such a breadth of product lines, or a large sales bag, that sometimes the smaller revenue-generating products are dismissed discontinued. And I believe that’s what happened with cryoplasty. But for our company, which is Gemini NuCryo, it’s a great opportunity because we’ve, in a relatively short period of time, reengineered the product twice from the inflation perspective and we’ve eliminated a ton of costs.

Scott Nelson:            To finish up on the story, you mentioned that back in 2014, Dr. Joye reacquired the assets from Boston Scientific. Do you know the underlying rationale? Was it based on the fact that he was involved initially with this product through Cryovascular?

Kevin Beedon:          Dr. Jooye was the founder of cryoplasty back in 1999. He’s always believed in the technology in addition to a lot of other physicians. So when the opportunity to buy back the assets came up, he jumped on it. And the team that we have today are individuals that were originally involved with Cryovascular as well as some other folks from Boston Scientific. The team that was formed were people that had experience with cryoplasty and they, along with Dr. Joye, were excited to work on it. So it was an opportunity to buy back the assets, reengineer it, make it more cost-effective in the market in order to compete head-to-head with other technologies. Plus, there’s some nice clinical data too.

Scott Nelson:            When you put all those pieces together, it really does make for an interesting opportunity on a lot of different fronts. Before we get into how you were able to move so fast from an R&D perspective, I want to ask you about the distribution agreement you had in place with Vascular Solutions. There are probably pros and cons with both avenues, so can you take us through the rationale to go direct versus continuing through a distribution channel?

Kevin Beedon:          First of all, Vascular Solutions is a great company with a proven track record of success. They have an impressive product portfolio and a specific sales model that’s worked very well for them. However, it was a mutual decision for us to part ways. We’re very excited about moving forward in this way because it gives us the opportunity to be in complete control of our future from both a sales perspective and from an engineering perspective. There are a lot of physicians that have used cryoplasty, it’s got a proven mechanism of action, it’s differentiated. We believe that going direct will allow us to engage the physicians and sort of reconnect them to this technology. It’s somewhat of a different sales model where we’re not trying to sell people on the data or sell someone on the device. What we’re really trying to do is reengage them and bring awareness to the COBRA study. Let them know that we’re back and they now have an opportunity to add cryoplasty back to their treatment algorithm. And because we’re such a small company, we’re very efficient and we’re super lean. And one of the things we emphasize is our cost control and our cost structure. Because we’re so lean and efficient, we can capitalize with a direct sales force in a market that’s ready and has been waiting for cryoplasty to come back.

Scott Nelson:            Makes a lot of sense when you explain the rationale because it would probably be entirely different story if you had to approach this more from a market development standpoint. Where you had to educate physicians not only on the product, but also on the disease state or maybe even the patient pathway. In your scenario, the device is proven and a lot of physicians are fond of it. So it allows for a lot of efficiency from a commercialization perspective.

Kevin Beedon:          Exactly.

Scott Nelson:            While on the topic of being lean and being able to iterate quickly at a lower cost, you were able to make changes to the product very quickly. In addition, your team was able to get regulatory clearance in short order as well. Things that are almost unheard of within large device companies. So are there some key takeaways that we can learn from in regards to how you approached this from a R&D and regulatory perspective?

Kevin Beedon:          I think it’s a real testament to the engineering team that was put together because the rights were acquired in August of 2014, and in a relatively short period of time, we had to find a facility, set up a clean room, create a manufacturing line, and start production. Remember, NuCryo Vascular went to market with the distribution model in early 2015. So all those steps had been completed within that timeframe.

Also, the 510(k) submission only took 40 days for approval. Because we have a lean team, we can get the engineering folks to do their work, we can analyze it and provide feedback very quickly. Dr. Joye can provide his input from the end-user’s perspective. And then we can go back and do it again. Not a lot of bureaucracy and a total team effort allowed us to really do something relatively quickly in today’s world.

Scott Nelson:            Regarding the regulatory submission taking only 40 days, does that speak to how it was initially submitted or the relationship with a particular FDA reviewer? Can you provide us with some additional details?

Kevin Beedon:          I think it was a combination of the history of cryoplasty as well as the modifications we made. There were modifications to the inflation unit that allowed it to be more effective and more cost-effective. The FDA asked a few questions and we responded relatively quickly. So the turnaround time from their response to ours was also something that we could do really fast because of the team we had in place. We try to be very efficient in all of our activities.

Scott Nelson:            I’ve got a friend that’s a regulatory consultant and she always scoffs at this notion that the FDA is always to blame. Maybe that’s the case in some scenarios. But she has mentioned to me several times that if the submission is tight and well done, that will save a ton of back and forth dialogue between the device company and the FDA. Seems like regulatory approvals can happen fast if they’re done well. So again, congratulations on how fast your team was able to accomplish that.

Before we transition to your career experiences, Kevin, let’s discuss the changes you’ve made to the PolarCath device and why a physician might be interested in using it now.

Kevin Beedon:          I think the basis for cryoplasty is its mechanism of action and apoptosis, or the biological effect that it provides. There’s not another balloon in the peripheral space that treats with the -10 degree Celsius cooling impact of apoptosis. So I think that’s critical for why physicians are excited that it’s back and why we’re excited to bring it back to market. But with the importance of price in today’s market, with our next-generation unit that we just got 510(k) approval for, it’s a nonsterile reusable device for up to 100 inflations. Prior to that, every time an inflation unit was used, it was disposed of after the case. And there was a cost associated with that for both the manufacturer as well as the hospital.

By introducing this next-generation unit, it significantly lowers the cost per procedure for PolarCath. So now we can talk to physicians, hospitals, office-based labs, office administrators, etc. and we have an economic story that will compete in today’s market. And again, we have proven data, the COBRA study, as well as an existing customer base. But it was absolutely critical for us to get the 510(k) approval to compete in today’s market.

Scott Nelson:            So the balloon itself is disposable, but the inflation device that allows for the cooling effect, that itself is reusable now.

Kevin Beedon:          Yes, you’re correct. The reusable inflation device is going to be significantly less per case because you can amortize the initial cost over 100 cases, or 100 inflations, which will allow us to compete with other specialty balloons on the market.

Scott Nelson:            Let’s now transition to your career, Kevin. You came up through the ranks on the sales side with Boston Scientific and Spectranetics Focusing on your most recent move from Spectranetics to Gemini and NuCryo, can you explain that transition in your career?

Kevin Beedon:          First of all, Spectranetics is a great company. I really enjoyed my time there. But when the opportunity with Gemini came to my attention, it was something I couldn’t turn down. It was a startup with great people, people that I admire and people that I knew I’d really enjoy working with. It was also based on a technology that I used to sell at Boston Scientific back in 2006. And I really believe there’s a market out there for it. With the COBRA study and the changes that I knew that were forthcoming, it seemed like a great opportunity to take a chance at a startup with a great team. It was almost too good to turn down and that’s why I eventually left Spectranetics,

Scott Nelson:            I’m sure some people would analyze that move and say, “Really exciting opportunity, but you’re taking a big risk.” So how did you justify balancing the pros and cons of making that move from Spectranetics to NuCryo and Gemini?

Kevin Beedon:          That’s a great question. Something my wife and I talked about. I certainly talked with my friends and some of my mentors about it. I did the analysis. Spoke with Dr. Joye and the team at NuCryo and Gemini. And once again, it came down to the opportunity that’s ahead of us as well my passion for the product.

I honestly don’t think there is another opportunity in the medical device space that we have right now at NuCryo Gemini. And it all comes down to the proven track record of the device, the data, the next-generation unit, etc. We don’t have to be everywhere in the market, we just have to be part of the algorithm for PAD and we will be successful. We also have a strong future at Gemini NuCryo from a product perspective. I get to work with really good people, like Dr. Joye, who I admire and I respect. I just had to say yes and I’m very happy that I did.

Scott Nelson:            As I mentioned before, you came up through the sales ranks and have held various sales leadership positions at Boston Scientific, Spectranetics, etc. But your undergrad is in chemical engineering, you’ve got an MBA in finance, so I’m curious as to why you stayed on the sales side through your career versus other positions that you probably could have taken within the medical device space that were maybe closer to your background. Whether it was a marketing position or whether it was something else. So why sales and how do you think that’s helped you along the way?

Kevin Beedon:          That’s a great question. After graduating with a chemical engineering degree, I worked for Dell Corning in the engineering space for three-plus years and then I transitioned over to marketing, I think that’s given me a broad foundation that applies to the medical device space. So there’s a technical component that I believe I bring to the sales model that’s helped me in my career. But more importantly, one thing that I truly love and enjoy is building teams. I love the human element. And so with sales, it allows me to engage physicians. To have difficult conversations about a technology that might be misunderstood or how they might consider it within their treatment algorithm. Sales is challenging, but also allows you to engage people, to build relationships with them, and provide them a product that will service them and their patients. So that’s why I’ve always enjoyed sales and that’s why I love the position I’m in right now.

Scott Nelson:            As you think back to your sales experiences versus what you’re doing now in your role as GM of NuCryo, are there things that you wish you had more experience in? People reading this interview might have opportunities to zig and zag throughout their career, to go from sales to marketing, marketing to medical education, etc. What are your thoughts about that?

Kevin Beedon:          First, I think you always have to surround yourself with good mentors that you trust. And for me, I’m fortunate my wife is also in the medical device space and so she’s a great sounding board. But I think at the end of the day, you always have to have a story. I get phone calls from a lot of people now that ask about making a career move and they always ask about their résumé. It’s definitely a critical component and one that people look at. But I think you always have to have a story to tell. And so if you look at mine, I’ve been very fortunate. My first medical device job was with Boston Scientific, as a peripheral sales rep, which happened to include cryoplasty. And that connected me with Dr. Joye and I believe this is one of the reasons why I’m here today. I was also allowed to launch a coronary stent before transitioning to Spectranetics. So as long as you make a change that makes sense to you and there’s a story behind it, I don’t think you should be afraid to take risks or to make certain changes. Just believe in that path and stay true to it. Change is inevitable but you have to manage through it and believe in the path that you’re on.

Scott Nelson:            So what’s next with NuCryo? You’re clearly excited about the opportunity you have with the new PolarCath device, but can you tell us a little bit more about what’s ahead for the company?

Kevin Beedon:          One of the great things about Gemini is that we’re really a medical device startup that was created to develop, engineer, manufacture, and distribute novel or new medical devices that are differentiated for the treatment of PAD. We already have prototypes and IP that we’re working on. And our goal is to develop them through collaboration with other entrepreneurs. In fact, other physicians have already contacted us about ideas they have. Because we’re such a small shop and we’re so efficient, we can take an idea, build a prototype, get voice-of-the-customer feedback, and then build a marketing plan around it. So that’s the future. Stay small, have a direct sales force, grow a little bit here and there, but always be nimble enough to adapt. We’re going to continue this process of bringing out new technology year after year after year.

Scott Nelson:            Is it safe to say that Gemini acts a little bit like an incubator or an accelerator specific to the peripheral vascular market?

Kevin Beedon:          Absolutely. That’s one way to look at it. There are various ideas and thoughts behind an incubator, but right now we have a business plan that’s lined up with a product we already want to bring to market in a few years. But first and foremost, our goal is get cryoplasty off the ground, get it back to where it was, produce a nice revenue stream, and then build off of that with the products that we already have in our pipeline.

Scott Nelson:            You obviously have a lot of experience in the peripheral vascular market. And as you know, it’s one that’s pretty competitive with a lot of different players that have solid sales forces and quality products. So when you look at how competitive this particular market is, what thoughts come to mind?

Kevin Beedon:          T peripheral space is highly competitive and there’s new competitors coming to market almost every day it seems like. But the one thing that I really appreciate when I talk to other sales reps at other companies is the focus that we’re going to have within our bag. With a lot of larger companies, they have to continue to add products because to the bag because their margins are dropping due to increased competition. But for us, we’re extremely focused. We have one product right now and we have a direct sales team that’s going to target a proven customer base. So I think that gives us a competitive advantage, which will hopefully prove to be true in the coming years.

Scott Nelson:            Let’s transition to one of my favorite parts of these interviews, which is more personal in nature. With that said, what’s your favorite nonfiction business book?

Kevin Beedon:          Thinking off the top of my head, it’s probably ‘Into Thin Air’, about the Mount Everest story. It’s a great story about survival. One that’s very engaging conquering Mount Everest.

Scott Nelson:            Second question, is there is a business leader, whether it’s a CEO or anyone else for that matter, that you’re following right now? Or maybe one that inspires you?

Kevin Beedon:          I’m a Michigan State grad and I’m a big Tom Izzo fan. I really respect what Tom Izzo has done. He’s built an amazing program. And I think that’s really critical in today’s medical device space. You have to build a program. That’s what really defines success. I think Tom Izzo has done that at Michigan State. He’s a motivator, a mentor, a teacher, and an absolute disciplinarian. He’s built a program that has a great culture where his players have fun. I’m a big fan of working hard, but at the end of the day, if you’re not having fun, I think you really have to look in the mirror and figure out, “Is this the opportunity for me?” It’s never going to be easy, but you have to enjoy what you’re doing. And I think that’s what Tom Izzo has done at Michigan Stae.

Scott Nelson:            Okay, so last question. When thinking about your career, even back to your days at Dell Corning, is there something that you would tell your 30-year-old self?

Kevin Beedon:          There’s probably a lot I would tell myself. But for the sake of this interview, I would tell myself to not be afraid to take some risks. Also, I think you need to surround yourself with good people that have your your best intentions in mind. And that’s not easy, but I think it’s critical. When I decided to make the move to Gemini, I talked to my peers inside the industry as well as friends and family outside the industry. I think you have to have a sounding board of people that have your back and will give you straight advice. Sometimes it hurts, but I think it’s important to hear. Change is important and it helps you grow. So take risks, but make sure you analyze everything appropriately.

Scott Nelson:            Great advice. To end our conversation, for people that want to learn more about Gemini Interventional or NuCryo, where would you direct them to?

Kevin Beedon:          I’d direct them to NuCryoVascular.com. They can also visit PolarCath.com or Cryoplasty.com if that’s easier to remember.

Scott Nelson:            Thanks so much for your time, Kevin.

Kevin Beedon:          Thanks Scott. I appreciate the opportunity.

Scott NelsonScott Neslon is a long time medtech enthusiast and founder of Medsider.com.

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Vivify Health raises $17m for remote monitoring

Vivify HealthRemote patient monitoring tech company Vivify Health said Wednesday it raised $17 million in a new round of financing to support its remote health monitoring tech.

The round was led by healthcare provider and insurer UPMC and joined by “several other of the nation’s largest health systems and health plans,” including Heritage Group and Ascension Ventures, as well as LabCorp and Envision Health, according to a press release.

“After an extensive evaluation of a number of companies, Vivify Health clearly stood out to us as the one best aligned to deliver patient-centered remote care across UPMC’s integrated payer/provider system. As we deliver care under an increasingly risk-based reimbursement model, we are excited to become a customer, development partner and investor in Vivify’s scalable population health management technology. Backing this kind of innovation to solve critical healthcare problems is at the heart of our mission at UPMC Enterprises,” UPMC Enterprises prez Tal Heppenstall said in a press release.

Vivify Health’s solutions allow insurance providers and organizations to conduct virtual care visits, communicate with patients and members and remotely monitor patient populations. The company said its platform is tailored to users of varying technological expertise.

“Vivify’s remote monitoring and communication technology is essential to making patients true partners in their care and providing the right services when and where they need them, increasingly at home. As an integrated healthcare delivery and financing system, we are focused on keeping patients well and out of the hospital, and that can happen only with affordable, easy-to-use technology like Vivify’s,” UPMC international veep Dr. Andrew Watson said in a prepared statement.

Vivify Health’s systems are used by more than 500 hospitals and payers, the company said, to monitor and engage patient populations of varying sizes. The company claims it was the 1st company to offer cloud-based solutions for mobile population health and chronic care management using consumer mobile devices.

“We are honored to partner with UPMC, one of the nation’s most prestigious health systems, to advance its mission to provide outstanding patient care and shape tomorrow’s healthcare with innovative population health technology. We look forward to helping UPMC achieve unprecedented outcomes for its patients as part of its commitment to patient-centered, affordable care,” Vivify Health CEO Eric Rock said in prepared remarks.

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APN Health wins 510(k) for 3D cardiac mapping system

APN Health

Electrophysiology tool developer APN Health said today it won FDA 510(k) clearance for its Navik 3D advanced cardiac mapping system.

The system from Pleasanton, Calif.-based APN Health is designed to give operating electrophysiologists or cardiologists real-time 3D catheter locations using 2D fluoroscopic images correlated with the electrical activation of the heart to create 3D maps.

“FDA clearance of Navik 3D represents a major milestone for APN Health’s team. We are proud that we’ve been able to develop a cost effective and simple technology that allows physicians throughout the world to more easily, accurately, and confidently complete their procedures. Looking forward, our proprietary digital image processing techniques and algorithms provide us with a remarkable platform from which to provide even greater functionality for electrophysiologists,” CEO Dr. Jasbir Sra said in a press release.

The Navik 3D produces maps that highlight locations with abnormal heart rhythms such as atrial fibrillation, the company said. APN Health claims it is the 1st system of its kind that does not require specialized equipment, and instead uses patient monitoring and fluoroscopic imaging already present in electrophysiology labs.

Clearance was supported by data demonstrating the system’s ability to accurately identify catheter locations in the heart and create 3D maps of the cardiac chamber of interest, the company said.

The system includes a workstation and iPad designed to display real-time 3D cardiac maps in a number of different formats.

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GI Dynamics, in the red, says it has enough gas for 2016

GI DynamicsGI Dynamics (ASX:GID) reported it has enough assets to continue through 2016 after reporting a rough fiscal year 2015, seeing sales shrink over 50% while net losses and losses per share trimmed down.

GI Dynamics reported losses of $35 million, or $3.71 per share, on revenue of $1.3 million. That amounts to a 27% drop in losses as sales shrunk 53.5% compared with 2014. The company said the reduced revenue, down 50% from last year, was due to its Endo trial which was shut down early last year.

The company reported that it has $21.7 million in total assets, down over 50% from last year, when the company reported assets amounting to $59.5 million

In August, GI Dynamics said it would slash its workforce by 46% by the end of 2015, cutting about 25 jobs, after a too-high rate of liver infections forced the halt of a U.S. clinical trial for its EndoBarrier weight loss device.

The Lexington, Mass.-based firm said it was making the cuts to cover the cost of shutting down the trial and to make sure it has enough cash “to ensure sufficient cash remains available to establish new priorities, continue limited market development and research, and to evaluate strategic options.”

After the cuts are implemented GI Dynamics said it expects to have roughly 29 full-time workers.

Lexington, Mass.-based GI Dynamics said last March that the FDA halted enrollment in the 325-patient Endo trial after some patients developed bacterial infections known as hepatic abscesses.

GI Dynamics, which sacked chief medical officer Dr. David Maggs for cause last June, said there were 7 cases of hepatic abscess in the trial, for an incidence rate of roughly 3.5%. That’s nearly double the 2% safety threshold, the company said, noting that the rate outside the U.S. is about 0.73% “based on experience with approximately 3,000 units shipped commercially since 2009.”

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FDA backs Endo’s Topas mesh to treat fecal incontinence

Astora Women's HealthThe FDA’s Gastroenterology and Urology Devices Panel of the Medical Devices Advisory Committee this week voted unanimously to back approval of Endo Health Solutions (NSDQ:ENDP) subsidiary Astora Women’s Health’s Topas mesh designed to treat fecal incontinence.

The synthetic mesh does not require a transvaginal approach, according to a Medscape report, but is implanted using 4 small incisions in a procedure that takes less than 30 minutes.

“The safety issues are addressed within the confines of the study, but specific panel members have concerns about the applicability more generally…and over longer periods of time,” panel chairman Dr. Mark Talamini said, according to Medscape.

The panel said the device is effective at reducing fecal incontinence episodes by at least 50%.

Past issues with the safety of transvaginal mesh devices affected the panel’s judgement and discussion of the Topas system.

In January the FDA, prompted by a significant increase in complaints about a type of surgical mesh used to treat pelvic organ prolapse in women, put the product under its most stringent level of review.

The federal safety watchdog said it re-classified the mesh from Class II to Class III and will require makers to go through its pre-market approval process for transvaginal POP procedures. The moves do not apply to mesh used in other indications, including stress urinary incontinence and abdominal POP repair, the FDA said.

Astora said it will limit Topas procedures to surgeons who have previously implanted the device or those who are participating in a proposed postapproval study, and said it is developing a training program for the devices.

The committee said training would be necessary but it would be difficult to judge how many cases it takes to reach a competent level. The board called for a registry to follow surgeons and patient outcomes with the Topas mesh.

The company said it is still not clear when the Topas sytem will be approved.

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Versago raises $1.7m for ‘reverse needle’ access port

Versago Vascular AccessVersago Vascular Access said today it received $1.7 million in seed funding from Primo Medical Group’s network of investors to support its “reverse needle” subcutaneous access port.

West Bridgewater, Mass.-based Versago, a spinoff of Primo Medical Group, has designed and developed a subcutaneous port to access the body’s bloodstream and anatomical cavities that collect serous or ascitic fluid, according to the company.

“No one could have ever imagined that subcutaneous port access could be simplified by having the needle advance out of the port body instead of into the body of the port. This will truly simplify port access,” Primo Medical Group prez & board chair Steve Tallarida said in a press release.

The tech provides a large bore, reusable, power injectable conduit directly into a patient’s bloodstream or other anatomical areas and could replace tech like ports, peripherally inserted centeral catheters and central venous catheters, the company said. The system replaces the typical port septum with a large bore conduit topped with removable dilating needle tips that are extnerally triggered, and the needle pierces the skin from the inside out.

“Because our products offer larger gauge cannulas, much higher flow rates can be achieved than the current standard of care. Those higher flow rates open up entirely new applications and will overcome some challenges in accessing the vasculature and other fluids in the body,” Versago CEO Andrea Patisteas said in prepared remarks.

The seed funding will be used to continue development of the Versago line of ports and to initiate regulatory review and for further testing. The company said it will begin discussions with potential strategic partners in early 2016.

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MassDevice.com +3 | The top 3 medtech stories for February 26, 2016

plus3-1x1

Say hello to MassDevice +3, a bite-sized view of the top three medtech stories of the day. This feature of MassDevice.com’s coverage highlights our 3 biggest and most influential stories from the day’s news to make sure you’re up to date on the headlines that continue to shape the medical device industry.

 

3. Mindray shareholders OK managers go-private buyout

MassDevice.com news

Shareholders in Mindray Medical voted to approve the $3.3 billion proposal that would see the Chinese medical device company’s managers take it private.

Mindray said the $28-per-share deal is expected to close in March. Some 77.3% of the total outstanding shares were voted in the poll, with 82.6% of those voting to approve the transaction. Read more


2. RIP medical device pioneer Alfred Mann

MassDevice.com news

Alfred Mann, a medical device entrepreneur who helped develop several groundbreaking technologies, died at age 90, shortly after stepping down from a pair of companies he founded.

Mann founded 17 companies over his 70-year career, in industries ranging from aerospace to medtech, according to the L.A. TimesRead more


1. Abbott cautions on potential issue with MitraClip heart implant

MassDevice.com news

Abbott warned surgeons earlier this month about a potential issue with its MitraClip after receiving 9 reports of problems that led to surgical interventions.

In a Feb. 4 urgent field safety notice, Abbott Vascular said the reports indicated that the delivery system for the MitraClip device, which is designed to repair the heart’s mitral valve, malfunctioned during implantation procedures. In 1 of the cases the patient died after the procedure due to “severe comorbidities,” according to the notice. Read more

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Integra LifeSciences ekes out Street-beating Q4 numbers

Integra LifeSciencesIntegra LifeSciences (NSDQ:IART) eked out some Wall Street-beating numbers for the 4th quarter and raised its outlook for 2016, prompting investors to send its share price up today.

Plainsboro, N.J.-based Integra posted profits of $15.0 million, or 39¢ per share, on sales of $241.2 million for the 3 months ended Dec. 31, 2o15, marking a -12.7% profit slide on sales growth of 10.1% compared with Q4 2014.

Adjusted to exclude 1-time items, earnings per share were 87¢, a penny ahead of the consensus on The Street, where analysts were looking for sales of $241.1 million.

Integra swung to a loss for the full year at -3.5 million, or -10¢ per share, on sales growth of 10.8% to $882.7 million compared with 2014. Adjusted EPS came in at $3.08, 3¢ under consensus. Analysts were looking for 2015 sales of $888.7 million.

“Strong growth in our regenerative portfolios drove full-year organic sales growth of 6.7%, at the high end of our guidance range,” president & CEO Peter Arduini said in prepared remarks. “These results helped drive gross margin improvement of 140 basis points to 67.5% for the full year. We are pleased with our 2015 results and are enthusiastic about our prospects for 2016.”

Integra boosted its guidance for the rest of the year, saying it now expects to report adjusted EPS of $3.35 to $3.50 on sales of $975 million to $1 billion.

“Strong organic growth and an improved product mix drove margin expansion, cash flow and earnings growth for 2015,” CFO Glenn Coleman said. “Our 2016 guidance for double-digit sales growth, strong earnings growth, as well as improvements in gross margin and free cash flow keep us on a path to achieve our long-term growth and profitability targets.”

Last year was a busy 1 for Integra. The company closed the spinout of its spine business in July 2015, creating  (NSDQ:SPNE), and acquired TEI Biosciences and TEI Medical for $312 million that same month. In August Integra floated a $200 million follow-on offering. And just this month Integra closed on the buyout of the U.S. rights to Tornier‘s Salto Talaris and Salto Talaris XT ankle replacements and Futura silastic toe replacements, as part of Tornier’s $3.3 billion merger with Wright Medical (NSDQ:WMGI).

IART shares were up 2.1% to $60.86 apiece in early afternoon trading today.

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FDA: Avg time to decision for PMAs at record levels

FDAThe FDA released a report today detailing its stats for Premarket Approvals and 510(k) applications for 2015 and the 1st 3 months of 2016, hitting a high water mark for its time to decision for PMAs.

The FDA reported a significant improvement in the average decision time for PMAs, which cover high-risk Class III devices, clocking in at 209 days. That’s a 20% improvement from last year’s average of 262 days, and the lowest time to decision on record with the organization.

The agency said its percentage of PMAs approved dipped to 91% in the 1st 3 months of 2016, a 7% fall from its record high 98% approval rate in 2015. The numbers are still 5% higher than they were in 2014 at 86%.

For simpler 510(k)s, the agency reported stable numbers in the 1st 3 months of 2016 at 85%. That’s the same as the FDA clocked in in 2015 and only 1% higher than its rate of approval in 2014.

The average amount of time to 510(k) decisions decreased 14%, falling from 127 days in 2014 to 109 days in 2015, the lowest time to decision the agency has seen since 2006.

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RIP medical device pioneer Alfred Mann | Personnel Moves

MassDevice.com Personnel MovesAlfred Mann, a medical device entrepreneur who helped develop several groundbreaking technologies, died yesterday at age 90, shortly after stepping down from a pair of companies he founded.

Mann founded 17 companies over his 70-year career, in industries ranging from aerospace to medtech, according to the L.A. Times.

After Johns Hopkins University researchers in 1969 asked him to help create a longer-lasting pacemaker, Mann turned his eye from the aerospace industry to medtech, according to the Times. In later years he founded several medical device companies, including MiniMed, which Medtronic (NYSE:MDT) acquired for $3.3 billion in 2001.

Mann also started Advanced Bionics, which helped pioneer the cochlear implant; Second Sight Medical (NSDQ:EYES) and its retinal implant for treating blindness; and pharmaceutical company MannKind (NSDQ: MNKD), which is working on an inhalable insulin product. In recent weeks he stepped down from his roles at Second Sight and MannKind, the newspaper reported.

“We are all deeply saddened by the loss of our founder, mentor and friend, Al Mann, a pioneering leader whose contributions and vision profoundly impacted the lives of so many and whose legacy will impact many more. Everyone he came in contact with was enriched and inspired by him. Personally, I am eternally grateful for Al’s generous guidance and support these last 16 years. At Second Sight, we all feel deeply honored to have worked alongside of and known such a remarkable person. The world is a little darker without his presence, but his spirit will live on in every blind person who is brought back into the light by our products,” Second Sight co-founder & chairman Dr. Robert Greenberg said in prepared remarks.

“Al has been a wonderful inspiration, not only to me, but to all the employees of MannKind. His kindness, generosity, and business acumen have influenced all of us with whom he has done business and charitable work over the years. He will be terribly missed by many, including the countless patients around the world with diabetes and other serious illnesses, whose lives he improved. I am thankful to have had a close relationship with Al, and will reflect on his counsel and guidance in the years to come. Our resolve is now stronger than ever to continue Al’s legacy of medical innovation, as a tribute to this remarkable man, who did so much to help mankind,” added MannKind CEO Matthew Pfeffer.

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