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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.
 
DeviceSientra Silicone Gel Breast Implants
Generic NameProsthesis, breast, noninflatable, internal, silicone gel-filled
Regulation Number878.3540
ApplicantTiger Aesthetics Medical, LLC
9779 S. Franklin Dr.
Suite 300
Franklin, WI 53132
PMA NumberP070004
Supplement NumberS043
Date Received07/22/2024
Decision Date08/12/2024
Product Code FTR 
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  
Sientra provided FDA with a detailed description and supporting documentation for implementation of a new fluid dispenser – the Nordson Ultimus I Fluid Applicator – to replace the Nordson Performus III Fluid Applicator used in the manufacture of the breast implants.
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