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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 NameZILVER PTX DRUG-ELUTING PERIPHERAL STENT
Classification Namestent, superficial femoral artery, drug-eluting
ApplicantCOOK MEDICAL INCORPORATED
PMA NumberP100022
Supplement NumberS003
Date Received12/13/2012
Decision Date02/15/2013
Product Code
NIU[ Registered Establishments with NIU ]
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 study protocol.
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