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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.
 
DeviceINTEGRA DERMAL REGENERATION TEMPLATE
Generic NameDevice, dermal replacement
ApplicantIntegra Lifesciences Corp.
105 Morgan Ln.
Plainsboro, NJ 08536
PMA NumberP900033
Supplement NumberS048
Date Received06/03/2015
Decision Date06/25/2015
Product Codes MDD MGR 
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  
QUALIFICATION OF A NEW METHOD FOR QUARTERLY STERILIZATION DOSE AUDITS FOR THE INTEGRA DERMAL REGENERATION TEMPLATE MANUFACTURED AT THE PLAINSBORO, NEW JERSEY, INTEGRA MANUFACTURING FACILITY.
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