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

MAUDE - Manufacturer and User Facility Device Experience

  • 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
 

 
 
6 records meeting your search criteria returned- Product Code: NRA Patient Problem: Inadequate Osseointegration Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BIOMET UK LTD. UNK BEARING BIOMET OXFORD LEFT MEDIAL AN 10/24/2023
BIOMET UK LTD. UNK FEMORAL BIOMET OXFORD CEMENTED 10/24/2023
BIOMET UK LTD. OXF TWIN PEG CMNTLS FMRL MD 10/23/2023
BIOMET UK LTD. OXF ANAT BRG LT MD SIZE 3 PMA 10/23/2023
BIOMET UK LTD. UNK CEMENTLESS OXF TIBIAL TRAY 09/27/2023
BIOMET UK LTD. OXF ANAT BRG RT MD SIZE 7 PMA 09/27/2023
-
-