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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.
 
DeviceMEMORYGEL BREAST IMPLANT
Generic NameProsthesis, breast, noninflatable, internal, silicone gel-filled
Regulation Number878.3540
ApplicantMENTOR CORP.
33 TECHNOLOGY DRIVE
IRVINE, CA 92618
PMA NumberP030053
Supplement NumberS031
Date Received09/16/2015
Decision Date02/12/2016
Product Code FTR 
Advisory Committee General & Plastic Surgery
Supplement TypeNormal 180 Day Track No User Fee
Supplement Reason Postapproval Study Protocol - OSB
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
Approval Order Statement  
Approval of the following changes to the post-approval study for the device: to enroll women with both MemoryGel and MemoryShape in a single study to address device specific and device class safety endpoints and updates to the study timeline.
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