Here's a look at some of the top regulatory stories for medical device companies this week: FDA panel issues aneurysm device recommendations; Burr introduces fast-track FDA bill; Medtronic wins EU approval for MRI-safe Activa DBS devices; FDA approves Siemens 3D breast tomo device; Maquet's TigerPaw II recall is Class I
FDA panel issues aneurysm device recommendations
April 21, 2015 by Brad Perriello
Food & Drug Administration (FDA), Getinge, LAAx Inc., Maquet Cardiovascular LLC, Medtronic, Siemens, U.S. Senate
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