dijous, 30 de juny del 2016

Luminex closes Nanosphere buy

Luminex pays $58m for NanosphereLuminex (NSDQ:LMNX) said today that it closed its buy of Nanosphere (NSDQ:NSPH) through the purchase of 45.3 million shares at $1.70 per share, offering up $76.9 million for the company.

The company said that in addition to the purchased shares, it sent notices of guaranteed deliver with respect to 953,173 shares, and that the merger was completed “without a vote of Nanosphere’s stockholders.”

“We are pleased to announce the completion of this transaction and welcome the Nanosphere team to the Luminex family. This transaction creates an exciting opportunity to enhance our 4 pillars of growth strategy by providing our customers with a wider array of products, increased support and services, and greater depth in both the molecular microbiology and diagnostic markets. Consistent with the prior full year revenue estimate of between $28 to $30 million dollars, we expect Nanosphere to contribute between $13 million and $16 million to our consolidated revenue in 2016, and we expect its revenue to continue to grow at an annualized rate well into the double digits.  We continue to enjoy strong momentum in our base business, and look forward to updating our formal 2016 revenue guidance on our second quarter earnings call,” CEO Homi Shamir said in a press release.

In May, Luminex said a 3rd-party offer for Nanosphere prompted it to raise its own $83 million bid for the company and its Verigene molecular diagnostics technology.

A week earlier, Luminex offered $1.35 per share for Nanosphere and said it would also pay off some $25 million of Nanosphere’s debt.

The company said a $1.50-per-share bid from an unnamed 3rd party moved it to up the ante on its own offer to $1.70 per share, taking the total deal value to $102 million.

Nanosphere is forecast to post 2016 sales of $28 million to $30 million this year. The company posted sales of $21 million last year and reported that 1st-quarter losses fell -11.3% to -$6.7 million, or -55¢ per share, on sales growth of 42.7% to $6.6 million.

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SRS Medical wins CE Mark for Spanner prostate stent

SRS MedicalSRS Medical Systems said yesterday it won CE Mark approval in the European Union for its Spanner temporary prostatic stent designed to be used as both an indwelling Foley catheter and an intermittent urinary catheter in male patients.

The Spanner device consists of a pair of anchors and a silicone tube and is designed to reduce resistance in the bladder neck and prostatic urethra without stenting the external sphincter, SRS said. It’s blind, anesthesia-free implantation procedure is similar to that for a Foley catheter, according to the company.

“The Spanner is proven to have significant impact on medical outcomes, and often has a transformational impact on patient quality of life. We are excited to receive this approval, and we look forward to working with our European partners to deliver the Spanner to the patients that will benefit from it the most,” said in a press release.

In March, SRS Medical said it won approval from South Korea’s Korea Food and Drug Administration for the Spanner.

Earlier this year in January, SRS said it won the FDA’s approval for a clinical trial of its Spanner prostate stent for an expanded indication, a temporary implant designed to replace indwelling and intermittent urinary catheters.

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MassDevice.com +5 | The top 5 medtech stories for June 30, 2016

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Say hello to MassDevice +5, a bite-sized view of the top five medtech stories of the day. This feature of MassDevice.com’s coverage highlights our 5 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.

Get this in your inbox everyday by subscribing to our newsletters.

 

5. Gecko Biomedical lands $1.6m loan for surgical adhesives

MassDevice.com news

Gecko Biomedical said today that it landed a $1.6 million, interest-free loan from Bpifrance for the surgical adhesives it’s developing.

Paris-based Gecko, which pulled down a $25 million Series A2 round in March, said the €1.4 million loan will go toward clinical trials in Europe aimed at winning CE Mark approval during the 1st half of 2017. Read more


4. Study: Initially CE Marked medical devices have higher recall rate

MassDevice.com news

U.S. medical devices which won CE Mark approval in the European Union prior to gaining FDA clearance have a nearly 3 times higher rate of safety alerts and recalls, according to a new study published in The BMJ.

Researchers, led by Harvard’s Thomas Hwang, examined press releases and announcements of approvals, as well as public FDA and European regulatory authority databases for U.S. approvals, safety alerts and recalls to gauge different rates of recalls and alerts dependent upon where the devices 1st won approval. Read more


3. JustRight Surgical wins FDA 510(k) for 3mm pediatric vessel sealing system

MassDevice.com news

JustRight Surgical said today it won FDA 510(k) clearance for its JustRight 3mm pediatric surgery vessel sealing system.

The Boulder, Colo.-based company touted the win as the 1st and only from the FDA for an electrosurgical device designed specifically for pediatric patients. Read more


2. Appeals court upholds patent win for Medtronic’s Cardiocom

MassDevice.com news

A federal appeals court yesterday upheld a win for Medtronic subsidiary Cardiocom in a patent battle with Robert Bosch Healthcare Systems.

The U.S. Court of Appeals for the Federal Circuit upheld rulings by the U.S. Patent & Trademark Office’s Patent Trial & Appeal Board that invalidated a trio of Bosch patents. Read more


1. Medical device companies fear parallel regulation after Brexit vote

MassDevice.com news

Medical Device companies fear that Britain’s exit from the European Union could result in a “parallel” regulatory system which would require them to file separate applications to access the U.K. and E.U markets, according to a new report from ScienceBusiness.

Only 2 weeks ago, the Environment, Public Health and Food Safety Committee of the European Parliament and Council’s Committee of Permanent Representatives voted to endorse new medical device and in vitro diagnostic regulations. Read more

The post MassDevice.com +5 | The top 5 medtech stories for June 30, 2016 appeared first on MassDevice.



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JustRight Surgical wins FDA 510(k) for 3mm pediatric vessel sealing system

JustRight SurgicalJustRight Surgical said today it won FDA 510(k) clearance for its JustRight 3mm pediatric surgery vessel sealing system.

The Boulder, Colo.-based company touted the win as the 1st and only from the FDA for an electrosurgical device designed specifically for pediatric patients.

“Pediatric surgeons have been requesting ‘right-sized’ surgical instruments and technologies for years. This pediatric indication for use of vessel sealing is the 1st of its kind. It further validates the truly unique technical advancements made by our development team. We are the only surgical device manufacturer to focus solely on pediatrics. Now surgeons and hospitals are recognizing the value we bring to caring for the smallest of patients,” CEO Russ Lindemann said in prepared remarks.

Data from testing of the device which was used in achieving regulatory clearance of the device was presented at the Society of American Gastrointestinal and Endoscopic Surgeons clinical congress in May, the company said.

The sealer is designed for use in extremely tight or small spaces found in teens, children, infants and neonates, JustRight said. The device allows for the permanent fusing of vessels, with low energy use designed to be safe for smaller patients.

In February, JustRight Surgical said it raised a total of $11.2 million in a Series B debt-and-equity round for its surgical stapler and sealing devices.

The Series B round, including $4.2 million in equity and $7 million in debt financing, is earmarked for furthering the U.S. and European commercialization of the company’s devices.

Founded in 2010, JustRight won 510(k) clearance from the FDA for the JustRight 5mm stapler in February 2014, billing it as “the smallest classic stapler on the market.” The company raised a $7.5 million round later that year, adding to the $10.5 million it drummed up in 2013.

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Leading the battle against sepsis: A MassDevice podcast with Spectral Medical CEO Paul Walker

Spectral Medical

Spectral Medical CEO Dr. Paul Walker has been focused on finding a solution to identify and treat sepsis, and specifically endotoxins that are known to trigger it, for over 20 years.

Sepsis affects approximately 1 million patients in the U.S. each year, and even more worldwide – and treating the deadly condition has proved to be a challenge for the healthcare industry. For Walker, it’s a challenge worth facing.

Walker holds a PhD in biochemistry and has held positions as 1st chief of critical care at the Toronto General Hospital, chief of surgery at the University Health Network and COO of Toronto General Hospital, but has always been intrigued by the challenge of identifying and treating sepsis.

During his time, Walker collaborated with a colleague to develop the only diagnostic assay which can identify endotoxin levels from whole blood – and joined Spectral to commercialize the device and strike out against sepsis.

Spectral Medical produces the Endotoxin Activity Assay to identify endotoxin levels and is the U.S. marketer of the Toraymyxin device – an investigational therapeutic hemoperfusion column designed to treat patients in septic shock with elevated levels of endotoxins.

Walker spoke to MassDevice about his efforts to take on endotoxins and sepsis at the head of Spectral Medical, and what’s next for the burgeoning medical device firm.

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Appeals court upholds patent win for Medtronic’s Cardiocom

Medtronic CardiocomA federal appeals court yesterday upheld a win for Medtronic (NYSE:MDT) subsidiary Cardiocom in a patent battle with Robert Bosch Healthcare Systems.

The U.S. Court of Appeals for the Federal Circuit upheld rulings by the U.S. Patent & Trademark Office’s Patent Trial & Appeal Board that invalidated a trio of Bosch patents.

Bosch had alleged that the electronic data collection system used with Cardiocom’s chronic disease management platform violated U.S. patents 7,516,192 (Networked system for interactive communication and remote monitoring of individuals), 7,840,420 (Multiple patient monitoring system for proactive health management) and 7,921,186 (Networked system for interactive communication and remote monitoring of individuals).

The PTAB ruled in January 2015 that the patents were unpatentable as obvious in light of prior art. Bosch appealed, but the Federal Circuit yesterday upheld the PTAB decisions without comment in a per curiam decision.

Fridley, Minn.-based Medtronic bought Cardiocom for $200 million in cash in August 2013 in a bid to get into the disease management business.

Chanhassen, Minn.-based Cardiocom makes devices aimed at helping to manage chronic conditions like diabetes or heart disease.

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Study: Initially CE Marked medical devices have higher recall rate

generic-hospital-or-1x1

U.S. medical devices which won CE Mark approval in the European Union prior to gaining FDA clearance have a nearly 3 times higher rate of safety alerts and recalls, according to a new study published in The BMJ.

Researchers, led by Harvard’s Thomas Hwang, examined press releases and announcements of approvals, as well as public FDA and European regulatory authority databases for U.S. approvals, safety alerts and recalls to gauge different rates of recalls and alerts dependent upon where the devices 1st won approval.

Data indicated that 67% of the 309 devices identified in the study were approved in both the U.S. and the EU, with 63% of those devices 1st winning CE Mark approval in the European Union.

Devices which won initial approval in the EU were associated with a 2.9 times greater rate of safety alerts and recalls, and a 4.6 times greater rate of recalls alone, according to the report.

“Devices approved first in the EU are associated with an increased risk of post-marketing safety alerts and recalls. Poor trial publication rates mean that patients and clinicians need greater regulatory transparency to make informed decisions about treatment,” authors wrote in the study.

Authors referenced a particular drug eluting stent, which won CE Mark approval in 2006, but was recalled 1 year later after the results of a U.S. pivotal trial showed the device was associated with “significantly increased rates of major adverse cardiac events, including myocardial infarction and target vessel revascularization.”

The higher rate of recalls and alerts could be a result of more strenuous testing required to hit the U.S. market, with the FDA maintaining stricter guidelines and requiring high risk devices to demonstrate “reasonable assurance of safety and effectiveness” before they can be used by patients. For the EU, devices can be marketed if they perform “as intended” and are likely to be safe, authors wrote.

“Patients and clinicians need access to, and balanced presentation of, the available evidence of the safety and effectiveness of novel devices, as well as clear communication about the evidentiary gaps. Our findings suggest that products introduced earlier in their development cycle are also more likely to increase the risk of harms, underscoring the urgent need for transparency to make truly informed decisions,” study authors wrote.

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FDA approves Concordia’s Photofrin 630 laser

Concordia InternationalConcordia International (NSDQ:CXRX) said it won pre-market approval from the FDA for its Photofrin 630 laser, which is designed to activate an anti-cancer drug in patients with throat and lung cancers.

Oakville, Ontario-based Concordia said the device is designed to activate the drug Photofrin (porfimer sodium) in patients with esophageal cancer, Barrett’s Esophagus and non-small cell lung cancer. The Photofrin 630 laser was re-engineered to include new controls and peripheral systems, the company said.

“We anticipate that these improvements could support greater adoption of PDT with Photofrin within the oncology community,” chairman & CEO Mark Thompson said in prepared remarks. “In addition, PMA approval for this new laser represents an important milestone in our global growth plans for this asset.”

Concordia said it’s also running a Phase III trial of Photofrin in treating a bile duct cancer called cholangiocarcinoma.

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Medical device companies fear parallel regulation after Brexit vote

European Union flagMedical Device companies fear that Britain’s exit from the European Union could result in a “parallel” regulatory system which would require them to file separate applications to access the U.K. and E.U markets, according to a new report from ScienceBusiness.

Only 2 weeks ago, the Environment, Public Health and Food Safety Committee of the European Parliament and Council’s Committee of Permanent Representatives voted to endorse new medical device and in vitro diagnostic regulations.

The approval paves the way for for the adoption of 2 new draft regulations by the end of 2016, though the new rules would not take effect for 3 years in relation to medical devices and 5 years for IVD. The regulations cover the design, manufacturing and clinical testing of medical devices and in vitro diagnostics, and will affect all device manufacturing and sales in the E.U.

Whether those regulations will now apply to products in the U.K. is still uncertain, according to the report from ScienceBusiness.

“From a business perspective it is hard to see an upside to the UK’s decision to leave the EU. Britain’s influence in the development of the European MedTech regulatory environment has been extremely positive and we now face an uncertain situation with possible regulatory divergence over time,” Cook Medical EMEA exec veep Bill Doherty told ScienceBusiness.

Currently, medical devices can be marketed throughout the E.U. with only CE Mark approval by any of the approximately 70 notified bodies which are overseen by national regulators.

“It’s a question of what they will be able to rescue from the wreckage. If a deal cannot be done, device manufacturers would need to go through approval twice, once for the U.K. market and once for the EU market, and I don’t see any value in that for anyone,” U.K. Health Research Authority research ethics advisor Hugh Davies told ScienceBusiness.

Davies said he expects the country will try to keep things “as harmonised as possible,” which would allow for the mutual recognition of U.K. and EU notified bodies, with the U.K. following the previously agreed upon rules and regulations.

“The U.K. MHRA has been incredibly influential in leading on so many aspects of how healthcare products are regulated. Now we are marginalized. We may be invited to the table but won’t have a voice,” Davies told ScienceBusiness.

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Report: Japan OKs Canon’s $6.5B Toshiba Medical buy, despite reservations

ToshibaAnti-trust regulators in Japan reportedly approved the $6.5 billion acquisition of Toshiba‘s (TYO:6502) medical device business to Canon (NYSE:CAJ), but warned about the deal’s questionable structure.

Toshiba managed to book the sale before the deal actually closed by setting up a holding company with just $300 in assets to skirt Japanese anti-trust regulations. Yesterday Japan’s Fair Trade Commission said the method may be in violation of antitrust laws, but declined to issue a fine and approved the deal anyway.

“Canon thought the deal would be approved without problem if they used this method,” FTC official Takeshi Shinagawa told reporters, according to Reuters. “This method should not be repeated by any companies and if they do in the future, they could get a red light.”

The FTC typically does not make public any warnings issued to companies over the merger process, Shinagawa added.

“We have made this particular warning public to show how serious we look at this method,” he said, explaining that the FTC approved the acquisition because it would not hurt fair competition among medical equipment makers in Japan.

The U.S. Justice Dept. and the SEC are also investigating the accounting practices at Toshiba’s U.S. businesses.

Canon declined to comment. A Toshiba spokesman said the company takes the warning seriously and will comply with rules for the notification of mergers set by the FTC.

Toshiba in March granted Canon exclusive negotiating rights to buy Toshiba Medical after a hotly contested auction. The ¥665.5 billion sale of Toshiba Medical Systems follows the February announcement that Toshiba would sell the entire medical equipment unit rather than just a controlling stake. A bidding war soon developed among a slew of private equity players and rival corporations. Toshiba has also said that it will either shut down or transfer all of its other healthcare businesses by the end of March.

The deal provided much-needed liquidity for Toshiba, which is facing mounting restructuring costs after a $1.3 billion accounting scandal. Toshiba Medical Systems put up sales of $3.60 billion (¥405.6 billion) during fiscal 2015, which ended in March of that year.

Fujifilm Holdings (TSE:4901), which lost out to Canon in the race to be picked as preferred bidder for Toshiba Medical Systems, questioned Toshiba on the asset transfer and the timing of the deal.

($1 = ¥102.7200)

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Gecko Biomedical lands $1.6m loan for surgical adhesives

Gecko BiomedicalGecko Biomedical said today that it landed a $1.6 million, interest-free loan from Bpifrance for the surgical adhesives it’s developing.

Paris-based Gecko, which pulled down a $25 million Series A2 round in March, said the €1.4 million loan will go toward clinical trials in Europe aimed at winning CE Mark approval during the 1st half of 2017.

“Bpifrance’s continuous support not only provides us with financial stability towards our future, but also is a testimony of the value of our biopolymers platform. As such, Bpifrance is a central stakeholder to our short, medium and long-term development,” CEO Christophe Bancel said in prepared remarks.

Founded in 2013 by famed MIT hydrogels pioneer Bob Langer and Dr. Jeff Karp of Boston’s Brigham & Women’s Hospital, along with Bancel and Bernard Gilly of the iBionext Network, Gecko is also working on a high-viscosity, hydrophobic, fast-curing polymer called GB-02 for cardiovascular reconstruction. When cured, the polymer is designed to form an elastic, biodegradable film.

(€1 = $1.11058)

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FDA approves Raindrop presbyopia inlay from ReVision Optics

ReVision OpticsReVision Optics won pre-market approval from the FDA yesterday for its Raindrop near vision inlay, a corneal implant designed to treat presbyopia.

The Raindrop is a microscopic hydrogel inlay placed in the cornea of the patient’s non-dominant eye during a 10-minute procedure to gently reshape the anterior curvature of the cornea to provide near and intermediate vision, Lake Forest, Calif.-based ReVision said.

“The outstanding clinical results that supported FDA approval of the Raindrop near vision inlay clearly show that patients who have difficulty with near vision due to presbyopia now have a new option to obtain excellent uncorrected vision at all distances,” president & CEO John Kilcoyne said in prepared remarks. “We anticipate commercializing Raindrop in the U.S. to the approximate 2,800 surgeons and 30 million potential patients through a direct field salesforce beginning in the 3rd quarter of 2016.

“We were very impressed by the effort and commitment of the FDA during the PMA approval process, as the agency met or exceeded every milestone during the interactive review of the Raindrop PMA,” Kilcoyne said. “ReVision Optics is also grateful for the leadership and support of Drs. Roger Steinert and Douglas Koch, the medical monitors of the clinical study, and to the dedicated investigators, their clinical coordinators and staff who contributed their time, talents and expertise throughout the 6-year study.”

The FDA said the Raindrop inlay is the 2nd such device it’s approved for treating presbyopia, following the April 2015 green light for the Kamra inlay made by AcuFocus.

“Given the prevalence of presbyopia and the aging of the Baby Boomer population, the need for near vision correction will likely rise in the coming years,” Dr. William Maisel, deputy director for science and chief scientist in the FDA’s Center for Devices & Radiological Health, said in prepared remarks. “The Raindrop near vision inlay provides a new option for surgical, outpatient treatment of presbyopia.”

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FDA Advisory Committee members and ‘appearance issues’

FDA VoiceBy: Michael Ortwerth, Ph.D.

FDA relies on its advisory committees as a source of independent scientific and technical expertise and advice on challenging public health issues. Most advisory committee members are appointed as “special government employees” (SGEs). Like regular government employees, these committee members are subject to Federal conflict of interest laws and regulations.

A lack of understanding about our selection and evaluation process has, at times, resulted in confusion and misunderstandings by the public.  We’ve been working to bring greater transparency to how the financial interests of committee members are evaluated.

In 2008, we published “Guidance for the Public, FDA Advisory Committee Members, and FDA Staff on Procedures for Determining Conflict of Interest and Eligibility for Participation in FDA Advisory Committees.” That guidance describes how we apply financial conflict of interest requirements.

What has not been previously addressed in guidance is something called “appearance issues.” Sometimes FDA advisory committee members who do not have interests and relationships that are financial conflicts of interest nevertheless have interests and relationships that may create the appearance that they lack impartiality. Appearance issues are addressed in a government-wide regulation regarding standards of ethical conduct for government employees at 5 CFR 2635.502(informally known as “Section 502”).

Some examples include:

  • When a member of the household works or is seeking to work for the sponsor with a product before the committee;
  • When a member has had past financial interests with the sponsor with a product before the committee; and,
  • When a member has a current consulting contract with a sponsor but the contract is not related to the product or issue before the committee.

We have recently published new draft guidance describing FDA’s procedures for evaluating appearance issues and how we determine whether to grant an authorization for a member with an appearance issue to participate in an FDA advisory committee.

Section 502 implements the ethical principle that a government employee should be impartial in performing their official duties, meaning that they must not give preferential treatment to any private organization or individual or use public office for private gain. To the extent that an advisory committee member’s performance of official duties might appear to benefit themselves or certain other individuals who are close to them, they must take appropriate steps to avoid an appearance of violating these ethical principles.

We also explain in the draft guidance the circumstances that FDA considers when determining whether an appearance issue may exist. We evaluate the circumstances and assess whether the interests, relationships, or circumstances would cause a reasonable person with knowledge of the relevant facts to question the advisory committee member’s impartiality in the matter before the committee. For example, if an advisory committee member serves on the board of directors of a nonprofit organization and that organization receives donations from the sponsor that is presenting before the committee, we review the details of the donation to determine whether the member should be cleared for service on the advisory committee.

FDA has flexibility and discretion in deciding whether an advisory committee member with an appearance issue should be authorized to participate in the advisory committee meeting. We evaluate whether the government’s interest in the advisory committee member’s participation outweighs the concern that a reasonable person may question the integrity of the agency’s programs and operations. If so, FDA may authorize the member to participate in the meeting.

Although FDA advisory committees provide advice and input to the Agency, FDA makes the final decisions.

The draft guidance is being issued for public comment before we issue a final guidance. Under Federal law, FDA is not permitted to disclose confidential information provided by advisory committee members related to appearance issues. But we are specifically requesting comments on whether the agency should request that advisory committee members voluntarily disclose if they have been granted an appearance authorization.

FDA is committed to ensuring that appropriate expertise and experience is brought to bear on the critical public health issues facing the agency. Often, we convene advisory committee meetings to obtain independent expert advice and perspective. At the same time, it is important that the process we use to screen advisory committee members for participation in meetings be as transparent as possible, and that we protect the credibility and integrity of advisory committee advice. We welcome your comments on how the agency can continue to meet these important goals.

fda-voice-ortwerthMichael Ortwerth, Ph.D,. is FDA’s Director of the Advisory Committee Oversight and Management Staff

 

 

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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dimecres, 29 de juny del 2016

MassDevice.com +5 | The top 5 medtech stories for June 29, 2016

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Say hello to MassDevice +5, a bite-sized view of the top five medtech stories of the day. This feature of MassDevice.com’s coverage highlights our 5 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.

Get this in your inbox everyday by subscribing to our newsletters.

 

5. ‘Donnie Brasco’ brother sues Zimmer

MassDevice.com news

A former sales rep for Zimmer Biomet – who is the brother of the FBI agent on whom the movie “Donnie Brasco” is based – yesterday filed a $15 million lawsuit accusing the orthopedics giant of firing him for his grand jury testimony against a doctor who was allegedly performing unnecessary knee replacements.

Dominick Pistone, the brother of former FBI legend Joseph Pistone, spent 25 years selling Zimmer products before the company fired him in June 2015, according to the lawsuit. In 2007, Dominick Pistone became aware that an unnamed physician, referred to as “Dr. X” in his complaint, was “performing numerous double knee replacements, well above the average … primarily for financial gain and not in the best interest of the patients,” using the OtisKnee implant then made by OtisMed. Read more


4. Entellus Medical pays $11m for Cogent’s XeroGel

MassDevice.com news

Entellus Medical said it paid $11 million in cash to acquire the XeroGel surgical sinus packing from Cogent Therapeutics.

“We are pleased to secure ownership of this best-in-class nasal dressing technology as well as solidify control of the supply chain and distribution to our physician customers. We are excited about the opportunity to leverage our world class engineering team to explore potential innovations and future research & development projects,” president & CEO Robert White said in prepared remarks. “This acquisition highlights our continued commitment to the ENT space and our efforts to provide products that deliver an optimal physician and patient experience.” Read more


3. Cardiovascular Systems settles kickbacks lawsuit for $8m

MassDevice.com news

Cardiovascular Systems yesterday said it agreed to pay $8 million and sign a corporate integrity agreement to settle a False Claims Act lawsuit based on allegations from a former sales rep that the company ran kickbacks and an off-label marketing scheme to boost sales of its orbital atherectomy devices.

The settlement, 1st announced in March, calls for the St. Paul, Minn.-based company to pay $3 million up front and the remaining $5 million in 11 quarterly installments beginning in January 2017. The company will pay a 1.8% annual interest rate on the unpaid portion of the settlement, CSI said. Read more


2. Baxter wins Health Canada nod for Amia peritoneal dialysis system

MassDevice.com news

Baxter said today that it won a nod north of the border for its Amia automated peritoneal dialysis system.

The Health Canada approval makes Amia the 1st automated peritoneal dialysis device cleared in the U.S. and Canada that includes voice guidance, touchscreen control and 2-way telemedicine features, Deerfield Park, Ill.-based Baxter said. Read more


1. Zoll Medical wins $400m contract with U.S. Defense Dept.

MassDevice.com news

Zoll Medical landed a contract with the U.S. Defense Dept. worth $400 million to supply vital signs monitors, the Pentagon said yesterday.

The 1-year deal includes 5 1-year extension options, according to a press release. There were 2 other bidders for the contract, which will see Zoll supply its vital signs monitors to the Army and Air Force, the Defense Dept. said. Read more

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Nico touts studies using BrainPath to treat hemorrhagic stroke

Nico Corp.'s BrainPathNico Corp today released data from 2 recently published studies which utilized its BrainPath Approach to treat hemorrhagic stroke, touting a 95% clot reduction and no mortalities associated with the device.

The BrainPath system uses a shunt and specially designed instrumentation to give surgeons access to the subcortical section of the brain. The device won 510(k) clearance from the FDA last June for treating primary and secondary brain tumors, vascular abnormalities, intraventricular tumors or cysts.

Data from the studies was published in the journals Neurosurgery and Operative Neurosurgery, the Indianapolis-based company said.

“The consistency of outcomes is a result of our dedication and the neurosurgeons’ willingness to attend advanced training courses held across the United States. During these 1-day events, physicians are educated on a unique minimally invasive parafascicular approach that allows for safe access and near complete evacuation, and they are taught techniques for managing the bleeding blood vessel so it doesn’t re-bleed after exiting the surgical site. The BrainPath Approach offers a predictable formula for predictable outcomes,” CEO Jim Pearson said in a press release.

Both studies, a prospective single-center study and retrospective multi-center study, reported only a single death that was unrelated to the company’s BrainPath approach, the company said.

Data from the studies indicated a 94% ate of functional recovery in patients who had functional mRS scores at follow-up between 0-3, indicating moderate disability while maintainting the ability to walk unassisted.

“Hemorrhagic stroke appears to be following in the footsteps of ischemic stroke, with these significant clinical advancements now being published in well-respected neurosurgery journals. What’s emerging is unique and there is no other technology available that allows for access to the brain using a trans-sulcal surgical approach. We can see the market of treatable patients evolving and getting larger for hemorrhagic stroke because now we can intervene quickly and stop the active bleed – something not possible before,” Pearson said in a prepared statement.

Nico said that data from both studies “validate the importance of appropriate patient selection and standardizing the approach to early surgical intervention of hemorrhagic stroke.”

“The inertia has been against aggressive surgical intervention for this disease, but there has also been a constant pressure for progress for this group of patients who have had very bleak recovery or survival odds. There has been a need to have data supporting this approach in order to take the big jump for changing how quickly we address hemorrhagic stroke and how we approach it. This is the first step,” Dr. Mark Bain of the Cleveland Clinic wrote in the prospective study published in Operative Neurosurgery.

The company said the results are consistent with a previous multi-center study of 39 patients which reported 90% clot reduction in 72% of patients, and a median GCS improvement from 10 to 14 with no mortalities as a result of the surgery.

In February, Nico Corp. said it raised $15 million of a hoped-for $18 million funding round, led by prior backers River Cities Capital Funds and the Rose-Hulman Institute of Technology, for its BrainPath neurosurgery device.

Nico said in a regulatory filing that 41 investors participated in the round, which nearly doubled its previous fundraising efforts.

The company said it plans to use the proceeds to grow its commercial footprint and conduct a study on using BrainPath for early surgical intervention in spontaneous intra-cerebral hemorrhages, compared with a “watch and wait” approach.

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HeartStitch touts 1st-in-human use in aortic valve surgery

 

HeartStitchStructural heart focused HeartStitch today touted the 1st-in-man use of the company’s HeartStitch technology in a transapical access and closure procedure at the National Cardiac Research Center in Astana, Kazakhstan.

The 2 procedures were performed by device inventor, HeartStitch co-founder and CEO Dr. Anthony Nobles and CMO Dr. Michael Mullen, the company said.

“This exciting technology will be an important step in facilitating the next wave of technology in treating structural heart disease that will require safe, effective and simple access and closure of the ventricular apex. I believe this is the next wave of technology in treating structural heart disease. The ability to be less invasive without introducing new mechanical devices into the patient’s heart by emulating the open surgical technique is always the best way, but often the most difficult to achieve. This new technology does just that. Over the next year our task will be to refine the procedure, technology, and technique of using the device so that it may be implemented by cardiac teams performing these life saving heart operations,” HeartStitch CMO Dr. Mullen said in a press release.

Patients were treated with HeartStitch technology in a transapical procedure to implant an aortic heart valve, the company said, with no complications reported. HeartStitch said that the procedure was a step towards moving critical heart procedures to percutaneous methods, as opposed to more dangerous open heart surgery.

“This is a historical day for all of us. Whenever we perform a 1st-in-man with one of our new technologies, we recognize that we are entrusted with not only the lives of these patients, but the hopes of tens of thousands of patients who in the future will rely on this procedure for their lives. As a scientist there is no greater measure of your work than the ability to save a life. As a businessman I am also proud of the impact this has had on the people of Kazakhstan, our partners in this development,” CEO Nobles said in a prepared statement.

In March, HeartStitch and Nobles Medical touted separate procedures utilizing cardiac sutures with the company’s Hearstitch ST and Noblestitch EL devices.

Nobles Medical Tech said that the NobleStitch EL device was used in the 1st percutaneous ASD closure and ASA repair and remodeling without the use of an implantable device.

The NobleStitch EL device closes the hole through a minimally invasive cardiovascular suturing procedure, the company said, with a routine cardiac catheterization procedure to secure the closure.

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AtriCure wins CE Mark for AtriClip Pro2 LAA occluder

AtricureAtriCure (NSDQ:ATRC) said today it won CE Mark approval in the European Union for the AtriClip Pro2 left atrial appendage exclusion system designed for minimally-invasive LAA occlusion procedures.

The AtriClip Pro2 system is designed with an ambidextrous locking and trigger-style clip closing mechanism, the West Chester, Ohio-based company said, as well as handle-based active articulation levers and a hoopless end effector.

“We are excited to bring the AtriClip PRO2 device to the European market. The US launch has been well received by our customers and we’re looking forward to the continued growth of the AtriClip franchise,” CEO Michael Carrel said in a press release.

In April, AtriCure said it won FDA 510(k) clearance for its AtriClip Pro2 and launched the device in the U.S.

In February, the company said it’s launching a clinical trial of its AtriClip left atrial appendage closure device, aiming to show whether the device reduces the incidence of post-operative atrial fibrillation after cardiac surgery to repair a structural heart defect.

AtriCure said the 1st patient in the 1-year Atlas trial was enrolled at PinnacleHealth Hospitals in Harrisburg, Pa. The study, which is slated to enroll up to 2,000 patients with a high risk of developing POAF, is designed to compare treatment with AtriClip in conjunction with a heart defect repair procedure to patients who undergo heart defect repair alone. It’s also designed to evaluate healthcare resource utilization between the 2 groups, AtriCure said.

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Biostage files for orphan drug designation for Cellspan artificial esophagus

BiostageOrgan regeneration specialist Biostage (NSDQ:BSTG) said it asked the FDA for orphan drug status for its Cellspan artificial esophagus.

If the request is granted, Holliston, Mass.-based Biostage, formerly know as Harvard Apparatus Regenerative Technology, would win 7 years of market exclusivity after FDA approval, plus tax credits and an exemption from the federal safety watchdog’s drug registration fees.

“This submission is the 1st step in our effort to secure orphan status for our Cellspan esophageal implant, which we believe has the potential to be a valuable option in the treatment of esophageal cancer. The Biostage team is executing on the key initiatives required to advance into human clinical trials for our esophageal implant product candidate, and we remain on track with our plan to conclude its pre-clinical development, to publish our large-animal study results and to execute our related good laboratory practices studies during Q3 and into Q4,” CEO Jim McGorry said in prepared remarks. “Our plan and goal is to file an investigational new drug application with the FDA by the end of the current year. Assuming approval on a normal time-frame, we believe that by this time next year our Cellspan esophageal implant should be in a human clinical pilot study.”

In May, Biostage floated $5 million worth of common stock to fund its R&D efforts. The pre-revenues company reported a net loss of -$2.5 million for the 1st quarter of 2016 and quarterly R&D expenses of $1.4 million. Its cash holding were worth $4.8 million.

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Echo Therapeutics launches pre-regulatory CGM component testing

Echo TherapeuticsEcho Therapeutics (NSDQ:ECTE) said today it began stand-alone component and integrated testing of its NextGen continuous glucose monitoring system prototypes and selected a clinical research organization to aid it in arranging a regulatory and clinical strategy.

The Iselin, N.J.-based company is developing a non-invasive, wireless CGM for use in the outpatient diabetes market and the fitness, weight loss and personal lifestyle wearable-health space

“I am excited about the progress our development team has made in the development and testing of the NextGen components and on integrating them into a system. We received very positive feedback from our demonstration of the NextGen self-exfoliator and app at the 2016 American Diabetes Association Scientific Sessions in New Orleans this month. We look forward to collaborating with our experienced CRO on the clinical development and regulatory pathway of our technology,” CEO Scott Hollander said in a press release.

Echo Therapeutics said it began hardware and software testing of its NextGen Exfoliator and bluetooth transmitter as well, and is continuing testing of the NextGen sensor element and hydrogel. Testing of the company’s API and software application have been completed.

Earlier this month, Echo Therapeutics said it won Institutional Review Board approval to expand testing of its non-invasive continuous glucose monitor, which can now include both pediatric and adult subjects.

Last July, Echo Therapeutics said it is moving its research lab from Franklin, Mass. to Littleton, Mass. and terminating its previous lease in the process.

The developer of wireless glucose monitors and wearable health and fitness devices said it paid $150,000 to break the lease on its previous 37,050 square foot research facility in Franklin. Echo Therapeutics relocated on July 3 to a smaller 10,132 square foot research facility in Littleton, Mass., according to an SEC filing from the company.

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Baxter wins Health Canada nod for Amia peritoneal dialysis system

Baxter's AmiaBaxter (NYSE:BAX) said today that it won a nod north of the border for its Amia automated peritoneal dialysis system.

The Health Canada approval makes Amia the 1st automated peritoneal dialysis device cleared in the U.S. and Canada that includes voice guidance, touchscreen control and 2-way telemedicine features, Deerfield Park, Ill.-based Baxter said.

“As a leader in home dialysis, Baxter is committed to understanding patients’ and clinicians’ needs, so we can provide innovative therapy options that are designed to support access to care where and when it’s needed,” Baxter Canada head Stephen Thompson said in prepared remarks. “Baxter’s Amia with Sharesource system is uniquely designed to help more patients self-administer home PD therapy and allow healthcare providers the ability to remotely manage their patients’ care.”

Baxter said it plans to start a pilot launch of the Amia device in Canada late this year. The device won 510(k) clearance from the FDA in October 2015.

Earlier this month, Baxter CEO Jose Almeida said the company is getting out of the home hemodialysis business, ceding the field to market leader NxStage Medical (NSDQ:NXTM).

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Avita taps IMS for BARDA economics study of ReCell

Avita MedicalAvita Medical (ASX:AVH) said today it tapped health economics group IMS Health to join in an study of its ReCell regenerative medical device to evaluate its economic benefits when used at U.S. burn centers.

The ReCell device is designed to use the patient’s own skin cells to treat a variety of skin issues, including burns, reconstructive and cosmetic procedures, the company said.

“We have data to show that ReCell is safe, and very effective in treating burns. What we must also demonstrate is how our approach, in conjunction with other treatments, can save public health bodies money, by getting patients out of hospital faster, and improving their outcomes. The IMS study will generate standard budget impact metrics vital to driving discussions on reimbursement and access,” Avita CEO Adam Kelliher said in a press release.

The study is being funded by BARDA through a $61.9m development and procurement contract, the company said, and is expected to take 6 to 8 months as it evaluates the potential cost savings from major interventions for burn treatments, including wound bed preparation, grafting and scar management.

“Burns remain the 4th most common trauma in the international community, and cause 1% of non-fatal injuries in the US. Although burn fatalities have fallen over time, effectively managing burns remains a challenge, with significant morbidity and mortality among burn patients. Potential effects include shock, infection, electrolyte imbalance, respiratory distress, incapacitation, disfigurement, pain, and psychological complications due to scarring and deformity,” IMS said in a prepared release.

IMS said that burns cost the U.S. medical system more than $1.5 billion annually, and that the costs could “increase significantly if there was armed conflict or a mass casualty event.”

This week, Avita Medical said that the U.S. Department of Health and Human Services extended its contract with the company to the tune of an extra $8 million to support the U.S. market approval and launch of its ReCell autologous cell harvesting device.

The company said the additional funds will support the company’s premarket approval application for ReCell, as well as for funding new initiatives to explore the benefits of ReCell for treating burns at U.S. burn centers under the company’s investigational device exemption.

Funds will also be used to bolster personnel at the company’s Northridge, Calif.-based location, with staff focused on regulatory, supply chain, quality systems, clinical support and reimbursement.

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Entellus Medical pays $11m for Cogent’s XeroGel

Entellus MedicalEntellus Medical (NSDQ:ENTL) said it paid $11 million in cash to acquire the XeroGel surgical sinus packing from Cogent Therapeutics.

“We are pleased to secure ownership of this best-in-class nasal dressing technology as well as solidify control of the supply chain and distribution to our physician customers. We are excited about the opportunity to leverage our world class engineering team to explore potential innovations and future research & development projects,” president & CEO Robert White said in prepared remarks. “This acquisition highlights our continued commitment to the ENT space and our efforts to provide products that deliver an optimal physician and patient experience.”

Plymouth, Minn.-based Entellus said it expects to post a net loss of -$21 million to -$29 million this year, on sales of $73.0 million to $77.0 million. Second-quarter losses are pegged at -$5.6 million to -$7.6 million, on sales of $17.8 million to $18.8 million. The XeroGel acquisition is forecast to have no effect on the bottom line this year, the company said.

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Zoll Medical wins $400m contract with U.S. Defense Dept.

Zoll MedicalZoll Medical landed a contract with the U.S. Defense Dept. worth $400 million to supply vital signs monitors, the Pentagon said yesterday.

The 1-year deal includes 5 1-year extension options, according to a press release. There were 2 other bidders for the contract, which will see Zoll supply its vital signs monitors to the Army and Air Force, the Defense Dept. said.

Japan’s Asahi Kasei (TYO:3407) in 2012 paid $2.3 billion to acquire Chelmsford, Mass.-based Zoll. Former CEO Rick Packer, who led Zoll for 13 years before overseeing the merger, was promoted in March to primary executive officer and charged with building the healthcare business into “a 3rd pillar” of the Asahi Kasei Group.

The conglomerate, which is also in the construction and chemical & fiber businesses, said the healthcare unit will consist of Zoll, Asahi Kasei Pharma, Asahi Kasei Medical and “future global healthcare companies.”

Packer, who’s presided over a doubling in sales at Zoll to more than $1 billion since the April 2012 merger, was also named non-executive chairman. Zoll also promoted president Jonathan Rennert to replace Packer as CEO, and moved international SVP Ernest Whiton into the president role.

Also in March, the company won approval from Japan’s Pharmaceuticals & Medical Devices Agency for its Thermogard XP temperature management system for patients in sudden cardiac arrest.

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Cardiovascular Systems settles kickbacks lawsuit for $8m

Cardiovascular Systems Inc.Cardiovascular Systems (NSDQ:CSII) yesterday said it agreed to pay $8 million and sign a corporate integrity agreement to settle a False Claims Act lawsuit based on allegations from a former sales rep that the company ran kickbacks and an off-label marketing scheme to boost sales of its orbital atherectomy devices.

The settlement, 1st announced in March, calls for the St. Paul, Minn.-based company to pay $3 million up front and the remaining $5 million in 11 quarterly installments beginning in January 2017. The company will pay a 1.8% annual interest rate on the unpaid portion of the settlement, CSI said.

The settlement, in which the company admitted no liability, also requires CSI to cover the plaintiff’s legal fees. The 5-year corporate integrity agreement requires CSI to maintain and expand its existing compliance programs and hire an independent review organization to audit its compliance with federal healthcare programs.

The FCA suit, filed in 2013 and unsealed 2 years later, accused CSI of inducing physicians to use its products by offering free, all-expense-paid training programs “followed by explicit demands by CSI employees that attendees use CSI products on future patients,” giving away product for free, 3rd-party referral channel marketing, and “sham Speaker Bureau payments for high-prescribers and others whom CSI sought to cultivate,” according to the complaint filed in the U.S. District Court for Western North Carolina.

Travis Thams worked for CSI as a district sales manager from 2012 to 2013, according to the complaint.

The lawsuit also accused the company of running an off-label promotion scheme to push sales of its unapproved 4 French catheter. It alleges that CSI also promoted its devices for use in areas of the body it’s not approved for, such as the coronary arteries, and for conditions such as chronic total occlusion for which it is not approved.

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China FDA proposes review process for high-priority medical device registration

Emergo GroupBy Stewart Eisenhart, Emergo Group

Chinese medical device regulators are seeking comment on a draft proposal for determining which devices qualify for the country’s high-priority review program, and in what order.

The China Food and Drug Administration (CFDA) has targeted domestic Class II devices and imported Class II and III devices in the proposal (link in Chinese); the regulator seeks to establish three review groups for determining which devices qualify for high-priority reviews.

Group 1 devices would include products that are part of China’s National Science and Technology Major Project or the National Key Technologies Research & Design Program. Reviews of Group 1 devices to determine whether they qualify for high-priority registration would take five business days.

Group 2 devices would include the following types of products:

  • Devices that diagnose or treat rare disorders and show significant clinical advantages over existing treatments
  • Devices that diagnose or treat malignant tumors and show significant clinical advantage
  • Devices to diagnose or treat diseases that afflict older populations or children and for which no effective treatment or diagnosis methods currently exist
  • Devices that are considered urgently needed and that have no existing predicates available on the Chinese market

The CFDA would convene expert panels on a monthly basis to determine which Group 2 devices qualify for high-priority review and which should undergo normal premarket review.

Group 3 devices would include other products that should be evaluated as high priority.

The CFDA first announced its high-priority review pathway in 2014 as a way to introduce innovative medical technologies into the Chinese market faster than through standard registration. While the high-priority pathway does not necessarily curtail any requirements of the standard CFDA registration process, it may nonetheless speed up review timeframes for qualifying manufacturers.

Emergo consultants in China will provide updates on the CFDA proposal in the near future.

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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dimarts, 28 de juny del 2016

‘Donnie Brasco’ brother sues Zimmer

Zimmer BiometA former sales rep for Zimmer Biomet (NYSE:ZBH) – who is the brother of the FBI agent on whom the movie “Donnie Brasco” is based – yesterday filed a $15 million lawsuit accusing the orthopedics giant of firing him for his grand jury testimony against a doctor who was allegedly performing unnecessary knee replacements.

Dominick Pistone, the brother of former FBI legend Joseph Pistone, spent 25 years selling Zimmer products before the company fired him in June 2015, according to the lawsuit. In 2007, Dominick Pistone became aware that an unnamed physician, referred to as “Dr. X” in his complaint, was “performing numerous double knee replacements, well above the average … primarily for financial gain and not in the best interest of the patients,” using the OtisKnee implant then made by OtisMed.

But that device was never approved by the FDA and eventually led to a 2-year prison sentence for OtisMed’s former CEO and an $80 million settlement for Stryker (NYSE:SYK), which acquired OtisMed in 2009.

“Pistone was very upset with what he saw happening to a large number of patients who were being treated by Dr. X, and who were being exposed to the products of OtisMed Corporation. Upon hearing Pistone’s concerns, his brother advised him to report the violations to the FBI,” he claimed in the complaint.

Pistone then took his concerns to the FBI, but declined to pursue the matter after an agent told him his anonymity could not be assured. He then called Zimmer’s internal whistleblower hotline, established as a part of a deferred prosecution agreement reaching in 2007 over alleged off-label marketing (earlier this month, federal prosecutors accused Zimmer of breaking their deal). There was no follow-up from Zimmer, the complaint alleged.

In June 2010 Dr. X joined an unnamed company and continued his practice of allegedly unnecessary knee procedures, Pistone alleged.

“Indeed, a large number of Company Y nurses and surgeons openly discussed Dr. X’s improper practices in the operating room,” according to the suit.

After a series of anonymous letters to a trio of Pennsylvania district attorneys and a newspaper drew no response, Pistone in February 2015 was subpoenaed by 1 of the DAs, for the Keystone State’s Northampton County, to testify before a grand jury about Dr. X’s alleged malfeasance.

After his March 2015 testimony, Pistone alleged, the CEO of Company Y threatened to sue Zimmer over the anonymous letters Pistone had written. Zimmer fired him June 15, 2015, claiming he had”diminished capacity,” and offered him a $200,000 severance deal that included a clawback option if it was discovered that he broke Zimmer’s conduct code, according to the complaint.

“Zimmer fired Pistone because he did exactly what [Zimmer’s code of conduct] indicated he was supposed to do – disclose violations of applicable law and/or Zimmer’s Code of Conduct,” according to the complaint.

Pistone is seeking $5 million in compensatory damages and $10 million in punitive damages.

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MassDevice.com +5 | The top 5 medtech stories for June 28, 2016

plus5-node

Say hello to MassDevice +5, a bite-sized view of the top five medtech stories of the day. This feature of MassDevice.com’s coverage highlights our 5 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.

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5. Sweden’s Handicare acquires mobility device developer Prism Medical

MassDevice.com news

Prism Medical said today that mobility and technical aid developer Handicare agreed to acquire it for approximately $62 million.

Swedish Handicare, which supplies technical aids for the elderly and physically disabled, will pay $12.50 for each outstanding share of Prism Medical. Read more


4. Unfazed by Brexit, PureTech launches Sonde voice diagnostics firm

MassDevice.com news

Life sciences incubator PureTech Health, unfazed by the worldwide impact of the U.K.’s vote to leave the European Union, announced its latest venture today: Sonde Health, which aims to use a voice-based technology to diagnose mental and physical ailments.

Based on technology licensed from the Mass. Institute of Technology’s Lincoln Laboratory, Sonde’s device is designed to analyze short vocal samples to screen for conditions based on acoustic changes. Read more


3. Wright Medical wants retrial in Conserve hip implant loss

MassDevice.com news

Wright Medical wants a federal appeals court to overturn the verdict in the 1st bellwether trial over its Conserve metal-on-metal hip implant, arguing that a new trial is warranted because the jury had 2 bites at the apple.

An Atlanta jury last year awarded plaintiff Robyn Christiansen $1 million in compensatory damages and another $10 million in punitive damages. The jury found Nov. 24 that the Conserve device was defective and that Wright failed to adequately warn patients about its risks. Read more


2. Mannkind taps medtech reps after Sanofi deal fails

MassDevice.com news

Mannkind chief commercial officer Michael Castagna is trying to resuscitate the inhaled insulin maker after its co-marketing agreement with Sanofi was cancelled at the beginning of the year due to disappointing sales. He’s fielding a team of about 70 people to sell the company’s Afrezza insulin inhaler, with about 13 coming from the medical device industry.

“We are looking to build a high energy nimble company that reflects the speed of the medical device industry, articulation of the science from biotech and a relentless focus on helping patients suffering from diabetes,” Castagna told FortuneRead more


1. Medtronic launches Beacon HF monitoring service

MassDevice.com news

Medtronic said today it launched its Beacon heart failure management service in the U.S., designed to monitor data from cardiac pacing devices to improve early interventions before heart failure events.

The service, which integrates data from the company’s implantable cardioverter defibrillator and cardiac resynchronization therapy devices, will allow patients to engage in daily health checks to both educate patients about conditions and to collect symptoms and biometrics. Read more

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CorMatrix lands CE Mark for CanGaroo surgical envelope

CorMatrixCorMatrix Cardiovascular said today that it won CE Mark approval in the European Union for its CanGaroo ECM surgical envelope for implanted cardiac devices.

Roswell, Ga.-based CorMatrix won 510(k) clearance from the FDA in August 2014 for the CanGaroo device, which is designed to act as a scaffold to stimulate natural wound healing using CorMatrix’s extra-cellular matrix. The CanGaroo envelope is meant to be used with implanted pacemakers and ICDs.

“With data trending toward increases in the number of implants in Europe, we’re excited to make this device available to the Electrophysiology communities of Europe,” president & COO Andrew Green said in prepared remarks.

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Report: Medtronic files for FDA approval of MiniMed 670G ‘artificial pancreas’

Medtronic's MiniMed 670GMedtronic (NYSE:MDT) has reportedly filed for pre-market approval from the FDA for its MiniMed 670G “artificial pancreas,” which is designed to automatically track and adjust blood sugar levels in patients with diabetes, and expects the federal safety watchdog to issue a decision within a year.

The device measures blood glucose every 5 minutes to keep patients within their target range, according to Bloomberg. Medtronic’s PMA bid is backed by a 124-patient trial that showed better blood glucose control than with manual testing and insulin administration. The average HbA1c blood sugar level at the start of the trial, 7.4, fell to 6.9 by the end of the study, with 58% of patients achieving that goal, the news service reported. There were no malfunctions, hyper- or hypoglycemic events or hospitalizations, lead investigator Dr. Richard Bergenstal, of Park Nicollet’s International Diabetes Center in Minneapolis, told Bloomberg.

Patients using the MiniMed 670G must still recalibrate the device every 12 hours, change out the glucose sensor weekly and refill the insulin reservoir every 3 days, but that’s still a vast improvement over hourly finger-stick tests.

“The work isn’t gone, but it seems to be a lot less,” Bergenstal said. “Patients are working 24 hours a day now. We want them to get control without spending every hour of the day worrying about their diabetes or preparing for the next event.”

“This was them, in their homes, going about their lives,” added Medtronic diabetes chief Francine Kaufman. “There was no remote monitoring. The closed loop is running the train now.”

The device proved so popular with the trial subjects that a group asked the FDA for continued access; the study went into an extended review period with more than 100 volunteers.

“It was totally mind-blowing,” Les Hazelton, who is 1 of the patients who joined the trial extension, told the newswire. “I like being in better control of my body and my disease. The more I know about what’s happening right now, the better I can manage it.”

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Gore touts Viabahn endoprosthesis superiority over PTA in new study

Gore's ViabahnW.L. Gore & Associates today released results from a clinical study of its Viabahn endoprosthesis in AV access graft outflow interventions, touting a 50% increase over percutaneous transluminal angioplasty alone in target lesion primary patency at 6 months.

The company reported that treatment with the Viabahn resulted in significantly better outcomes when compared against PTA alone for treating challenging AV access cases, both in terms of primary patency and number of interventions during the study period.

Results from the study were published in the Journal of Vascular Surgery, Newark, Del.-based Gore said.

“Patients with failing dialysis circuits that are unresponsive to balloon angioplasty are a real problem for physicians. Historically, angioplasty has been a popular treatment option, but our study found its 6-month primary patency rates to be well below the ‘reasonable goal’ of 50% stated by the 2006 K/DOQI Guidelines for Vascular Access. The data shown in the Gore Revise clinical study manuscript makes a compelling argument for Gore Viabahn Endoprosthesis use in those challenging cases,” primary author Dr. Thomas Vesely of St. Louis, Mo.’s Vascular Access Services said in a prepared statement.

Data from the study also indicated a 47% improvement in target lesion primary patency and a 48% improvement in circuit primary patency when compared against PTA alone at 6 months. In elbow placements, data indicated a 72% target lesion primary patency at 6 months and 83% access secondary patency at 24 months.

Median time to target lesion reintervention or graft abandonment with the Viabahn was reportedly 2 times that of PTA alone, and placement of the Viabahn led to 27% fewer interventions at the target lesion and in the dialysis access circuit over 2-years, when compared to PTA.

“The Gore Revise clinical study was the clinical support used to gain the U.S. on-label indication for Gore Viabahn endoprosthesis in AV access. By expanding indications to include AV access, Gore Viabahn endoprosthesis continues to show how physicians can depend on the device for complete coverage in complex cases,” Gore peripheral interventional biz leader Ray Swinney said in a press release.

Last December, Gore said it launched a post-approval study of its Viabahn stent graft. The 108-patient Reline Max study will examine the treatment of in-stent restenosis in the superficial femoral artery using the Viabahn device, which is designed to inhibit blood clots with its heparin coating.

The Viabahn stent graft, which 1st won FDA approval in 2005, was approved by the safety watchdog for treating in-stent restenosis last year.

The Reline Max trial’s primary safety endpoint is procedure- and device-related serious adverse events at 30 days, according to ClinicalTrials.gov, and the primary efficacy endpoint is primary patency without repeat intervention after a year. The trial, estimated to be complete in November 2020, is slated for final data collection in November 2018.

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Insurer launches trial of Avinger’s Pantheris atherectomy device

Avinger PantherisAvinger (NSDQ:AVGR) said yesterday that it is collaborating with health insurers Highmark Health and Allegheny Health Network to launch a trial of its Pantheris image-guided atherectomy device designed for treating peripheral artery disease.

The Pantheris device is designed to use optical coherence tomography to allow physicians to visualize the vessel and obstruction during atherectomy procedures to treat peripheral artery disease.

“Using this technology, we now have the ability to clearly see our way through the artery. This means there is less risk of damaging the artery walls, which can lead to an aggressive healing-and-scarring process that increases the risk of restenosis, or a re-narrowing of the artery after treatment,” Allegheny Health Network vascular surgery director Dr. Satish Muluk said in prepared remarks.

The partnership, and the study, are part of Highmark Health’s “verification of innovation by testing, analysis and learning” – known as Vital – innovation program, Avinger said. The program plans to evaluate the Pantheris device in terms of benefits to patients, providers and payers through the “holistic” evaluation of patient care, the company said.

“PAD is not an isolated problem. It is part of a disease spectrum that often involves diabetes, high blood pressure, cardiac abnormalities and renal insufficiencies. Accordingly, optimal PAD therapy should aim to understand, treat and improve both local and systemic disease effects. By linking delivered care with claims data in a collaborative environment, Vital is changing the conversation about episodic care and redefining what quality means,” Avinger CMO Dr. Arjun Desai said in a press release.

The Vital study will evaluate PAD patients treated with both the Ocelot and Pantheris lumivascular catheter devices, with acute and long-term outcomes compared against a historic cohort of both endovascular and surgical therapies, Avinger said.

A follow-up study will include claims data analysis investigating the evolution of the patient and related co-morbidities during the post-treatment period, the company said.

“Vital’s mission is to support bringing safe, innovative technologies to members and patients that increase quality of care and lead to better patient outcomes without undue financial burden. As one of the largest integrated health care delivery and financing systems in the nation, we embrace our responsibility to accelerate the pace with which novel technologies and services are made available to the public,” Highmark Health CEO David Holmberg said in a prepared statement.

In March, Avinger launched a new version of its Pantheris peripheral atherectomy device and registered for the sale of up to $50 million worth of its stock.

Redwood City, Calif.-based Avinger said the deal with Cowen & Co. doesn’t oblige it to sell any shares. Earlier in March, the company said it would immediately launch an enhanced version of the Pantheris device after winning FDA clearance. Pantheris won its 1st nod from the agency in October 2015; Avinger said the new version features improved ergonomics, physician controls and manufacturability.

Avinger floated a $65 million initial public offering in January 2015. Last September the company pulled in a $55 million term loan.

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