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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.
 
DeviceMENTOR SALINE-FILLED AND SPECTRUM BREAST IMPLANTS
Generic NameProsthesis, breast, inflatable, internal, saline
Regulation Number878.3530
ApplicantMentor Worldwide, LLC
33 Technology Dr.
Irvin, CA 92618
PMA NumberP990075
Supplement NumberS030
Date Received11/25/2014
Decision Date12/15/2014
Product Code FWM 
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  
CHANGE TO AUTOMATE THE EXISTING SILICONE ELASTOMER SHEET CUTTER USED TO CUT PART COMPONENTS FOR MENTOR SALINE-FILLED AND SPECTRUM BREAST IMPLANTS, MENTOR MEMORYGELSILICONE GEL-FILLED BREAST IMPLANTS AND MENTOR MEMORYSHAPE BREAST IMPLANTS MANUFACTURED ATMENTOR'S IRVING, TEXAS FACILITY.
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