• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Premarket Approval (PMA)

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back to Search Results
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.
 
DeviceNatrelle Saline Filled Breast Implants
Generic Nameprosthesis, breast, inflatable, internal, saline
Regulation Number878.3530
ApplicantAllergan
2525 dupont dr.
irvine, CA 92612
PMA NumberP990074
Supplement NumberS045
Date Received03/15/2021
Decision Date10/27/2021
Product Code FWM 
Advisory Committee General & Plastic Surgery
Supplement Typenormal 180 day track
Supplement Reason labeling change - indications/instructions/shelf life/tradename
Expedited Review Granted? No
Combination ProductNo
Approval Order Statement  
Approval for changes to the patient and physician labeling including a boxed warning and a patient decision checklist.
Approval OrderApproval Order
-
-