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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 NameCORDIS CYPHER SIROLIMUS-ELUTING CORONARY STENT
Classification Namecoronary drug-eluting stent
ApplicantCORDIS CORPORATION
PMA NumberP020026
Supplement NumberS042
Date Received09/06/2007
Decision Date10/16/2007
Product Code
NIQ[ Registered Establishments with NIQ ]
Advisory Committee Cardiovascular
Supplement Typenormal 180 day track no user fee
Supplement Reason labeling change - other
Expedited Review Granted? No
Combination Product Yes
Approval Order Statement 
Approval for revisions to the instructions for use.
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