Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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) | Registration & Listing | Adverse Events | Recalls | PMA | 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 has supplements. The device description may have changed. Be sure to look at the supplements to get an up-to-date view of this device.
 
Trade NameFIBREL
Classification Nameimplant, dermal, for aesthetic use
Generic Namegelatin matrix implant
ApplicantMENTOR CORP.
PMA NumberP850053
Date Received07/31/1985
Decision Date02/26/1988
Withdrawal Date 02/28/2008
Product Code
LMH[ Registered Establishments with LMH ]
Docket Number 88M-0094
Notice Date 05/03/1988
Advisory Committee General & Plastic Surgery
Expedited Review Granted? No
Combination Product No
Supplements: S001 S002 S003 S004 
-
-