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U.S. Department of Health and Human Services

Premarket Approval (PMA)
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Note: this medical device record is a supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device.
 
Trade NameATS 3F AORTIC BIOPROSTHESIS MODEL 1000
Classification Nameheart-valve, non-allograft tissue
ApplicantATS MEDICAL, INC.
PMA NumberP060025
Supplement NumberS005
Date Received05/14/2010
Decision Date07/13/2010
Product Code
LWR[ Registered Establishments with LWR ]
Advisory Committee Cardiovascular
Supplement Typenormal 180 day track no user fee
Supplement Reason postapproval protocol or modification to a protocol
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval of the post-approval protocol.
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