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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.
 
DevicePALMAZ BALLOON EXPANDABLE STENT
Generic NameSTENT, RENAL
ApplicantCordis US Corporation
14201 NW 60th Ave.
Miami Lakes, FL 33014
PMA NumberP890017
Supplement NumberS009
Date Received05/26/2000
Decision Date07/11/2000
Product Code NIN 
Advisory Committee Cardiovascular
Supplement TypeSpecial (Immediate Track)
Supplement Reason Labeling Change - Indications/instructions/shelf life/tradename
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
Approval Order Statement  
APPROVAL FOR A REVISED INSTRUCTIONS FOR USE (IFU) FOR THE CORDIS PALMAZ(TM) BALLOON EXPANDABLE STENT.
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