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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.
 
DeviceSupera Peripheral Stent System, Supera Pro Interwoven Peripheral Stent System
Generic NameSTENT, SUPERFICIAL FEMORAL ARTERY
ApplicantAbbott Vascular (Idef Technologies Inc)
3200 Lakeside Dr.
Santa Clara, CA 95054
PMA NumberP120020
Supplement NumberS020
Date Received09/05/2018
Decision Date10/04/2018
Product Code NIP 
Advisory Committee Cardiovascular
Supplement Type30-Day Notice
Supplement Reason Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
Approval Order Statement  
Increase the sterilization load density with a modified configuration.
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