Category — 510(k)
FDA Taking Comments on Potential New Hurdles for Approval of Medical Devices
[This post comes to us from Diane Romza-Kutz , Robert E. Browne, Jr., John F. Costello, Jr. and Matthew M. Morrissey of Troutman Sanders' Life Sciences Practice Team. We thought it might be of interest to our readers.]
Sept. 12, 2011 - The recent furor in the medical device industry over a new recommendation that the U.S. Food & Drug administration abandon its approval process for medical devices has prompted a new round of public meetings and comment. This provides a critical opportunity for the medical device industry to comment on these potential new hurdles to market entry. [Read more →]
September 12, 2011 Comments Off
