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

Manufacturer and User Facility Device Experience (MAUDE)

  • 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
 

 
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 > 
 
65 records meeting your search criteria returned- Product Code: NRA Patient Problem: Arthritis Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. UNKNOWN KNEE 10/02/2017
BIOMET UK LTD. UNKNOWN OXFORD KNEE BEARING 08/10/2017
BIOMET UK LTD. UNKNOWN OXFORD KNEE FEMORAL COMPONENT 08/10/2017
BIOMET UK LTD. UNKNOWN OXFORD KNEE TIBIAL TRAY 08/10/2017
BIOMET ORTHOPEDICS OXF ANAT BRG LT MD SIZE 5 PMA 02/03/2016
ZIMMER BIOMET, INC. UNKNOWN OXFORD KNEE 07/23/2015
BIOMET ORTHOPEDICS UNKNOWN KNEE 07/21/2015
BIOMET ORTHOPEDICS UNKNOWN OXFORD PARTIAL KNEE 07/20/2015
ZIMMER BIOMET, INC. UNKNOWN KNEE 07/20/2015
BIOMET ORTHOPEDICS UK UNKNOWN 05/27/2015
-
-