Here's a look at some of the top regulatory stories for medical device companies this week: FDA yanks enhancement reporting requirement; FDA approves Medtronic's full-body MRI-safe lead; FDA strikes out again in Prevor drug-or-device case; Abbott inks co-distribution deal with Carl Zeiss Meditec; Boston Scientific wins CE Mark for Accolade MRI-safe pacemakers
FDA yanks enhancement reporting requirement
October 15, 2014 by Brad Perriello
Abbott Medical Optics, Boston Scientific, Carl Zeiss Meditec, Food & Drug Administration (FDA), Medtronic, Prevor, Abbott Laboratories, AdvaMed
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