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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 PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information.
 
DeviceGORE VIABAHN ENDOPROSTHESIS
Classification Namestent, superficial femoral artery
Generic Namestent, superficial femoral artery
Applicant
W.L. GORE & ASSOCIATES,INC
3450 west kiltie ln.
p.o. box 500
flagstaff, AZ 86002-0500
PMA NumberP040037
Supplement NumberS012
Date Received11/20/2008
Decision Date01/26/2009
Product Code
NIP[ Registered Establishments with NIP ]
Advisory Committee Cardiovascular
Supplement Type30-day notice
Supplement Reason process change - manufacturer/sterilizer/packager/supplier
Expedited Review Granted? No
Combination Product Yes
Approval Order Statement 
CHANGE TO THE EPTFE CUTTING PROCESS.
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