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Biomet, Inc. - Testimony

Document ID: FDA-2011-N-0556-0014
Document Type: Public Submission
Agency: Food And Drug Administration
Received Date: September 27 2011, at 12:00 AM Eastern Daylight Time
Date Posted: October 7 2011, at 12:00 AM Eastern Standard Time
Comment Start Date: August 12 2011, at 12:00 AM Eastern Standard Time
Comment Due Date: September 30 2011, at 11:59 PM Eastern Standard Time
Tracking Number: 80f35b04
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This is comment on Notice

Center for Devices and Radiological Health 510(k) Clearance Process; Recommendations Proposed in Institute of Medicine Report: ‘‘Medical Devices and the Public’s Health, The FDA 510(k) Clearance Process at 35 Years;’’ Public Meeting

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The presentation given at the September 16, 2010 public hearing is submitted for further consideration

Attachments:

Biomet, Inc. - Testimony, Comments on the IOM Report on the 510(k) Process (091611

Title:
Biomet, Inc. - Testimony, Comments on the IOM Report on the 510(k) Process (091611

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Total: 21

Colorado Bioscience Association - Comment
Public Submission Posted: 10/07/2011 ID: FDA-2011-N-0556-0013

Comment Period Closed
Sep 30,2011 11:59 PM ET

Biomet, Inc. - Testimony
Public Submission Posted: 10/07/2011 ID: FDA-2011-N-0556-0014

Comment Period Closed
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American College of Cardiology - Comment
Public Submission Posted: 10/07/2011 ID: FDA-2011-N-0556-0015

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Arizona Bioindustry Association - Comment
Public Submission Posted: 10/07/2011 ID: FDA-2011-N-0556-0019

Comment Period Closed
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LifeScience Alley - Comment
Public Submission Posted: 10/07/2011 ID: FDA-2011-N-0556-0020

Comment Period Closed
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