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Findings From Largest Industry Assessment of 510(k) Process to be Released on May 24, 2011
Date:5/18/2011

erate a respondents' panel comprising Susan Alpert, MD, PhD, recently retired senior vice president and chief regulatory officer at Medtronic; Peter Barton Hutt, senior counsel at Covington & Burling LLP, author of the Medical Device Amendments of 1976; and Philip J. Phillips, president of Phillips Consulting Group LLC and former deputy director for science and regulatory policy in the Office of Device Evaluation at FDA's Center for Devices and Radiological Health. Senior leadership from FDA has been invited to participate.

Where:  Zenger Room, The National Press Club, 529 14th Street NW, Washington, DC

The news conference will be broadcast live via the web at: www.inhealth.org/510ksurveyWhen:  Tuesday, May 24, 8:30 a.m. to 10:30 a.m. Contact:Robyn Stein, gabbegroup, (212) 220-4444, robyn.stein@gabbe.com Caitlin Hool, gabbegroup, (212) 220-4444, caitlin.hool@gabbe.com   For more information about the survey, visit www.510k.net

About InHealth (www.inhealth.org)

The Institute for Health Technology Studies is a nonprofit research and educational organization supporting independent analyses of the social and economic effects of diagnostic and therapeutic medical devices.  


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SOURCE The Institute for Health Technology Studies (InHealth)
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