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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 NameXIENCE PRIME/ XIENCE PRIME LL / XIENCE EXPEDITION/ XIENCE EXPEDITION SV AND LL EVEROLIMUS ELUTING CORONARY STENT SYTEM
Classification Namecoronary drug-eluting stent
ApplicantABBOTT VASCULAR
PMA NumberP110019
Supplement NumberS040
Date Received01/24/2013
Decision Date02/20/2013
Product Code
NIQ[ Registered Establishments with NIQ ]
Advisory Committee Cardiovascular
Supplement Type30-day notice
Supplement Reason process change: manufacturing
Expedited Review Granted? No
Combination Product Yes
Approval Order Statement 
Shorten the shelf-life of a solvent used for the manufacturing of the devices.
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