National Medical Device Postmarket Surveillance Plan
MedSun: Newsletter #77, October 2012

The FDA is making available for public comment a preliminary report entitled "Strengthening Our National System for Medical Device Postmarket Surveillance." This report, in addition to providing an overview of FDA's medical device postmarket authorities and the current U.S. medical device postmarket surveillance system, proposes four specific actions, using existing resources and under current authorities, to strengthen the medical device postmarket surveillance system in the United States.

Additional Information:

National Medical Device Postmarket Surveillance Plan. September 6, 2012.

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