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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.
 
DeviceSEPRAFILM ADHESION BARRIER & SEPRAFILM PROCEDURE PACK
Generic NameBarrier, absorbable, adhesion
ApplicantBaxter Healthcare Corporation
One Baxter Pkwy.
Deerfield Lake, IL 60015
PMA NumberP950034
Supplement NumberS023
Date Received02/25/2003
Decision Date03/25/2003
Product Code MCN 
Advisory Committee General & Plastic Surgery
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  
THE RETURN OF DISTRIBUTION ACTIVITIES FOR SEPRAFILM ADHESION BARRIER AND SEPRAFILM PROCEDURE PACK TO THE FRAMINGHAM, MASSACHUSETTS, MANUFACTURING FACILITY.
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