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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 NameTRIFECTA VALVE
Classification Nameheart-valve, non-allograft tissue
Generic Nametissue heart valve
ApplicantST. JUDE MEDICAL, INC.
PMA NumberP100029
Supplement NumberS013
Date Received04/05/2012
Decision Date06/29/2012
Product Code
LWR[ Registered Establishments with LWR ]
Advisory Committee Cardiovascular
Supplement Typereal-time process
Supplement Reason process change: manufacturing
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval for a change to the trifecta valve stent specification to require 100% inspection for wall thickness at a new, single location - stent rail.
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