• 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
 

 
 < 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 > 
 
234 records meeting your search criteria returned- Product Code: KWA Patient Problem: Death Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER, INC. UNKNOWN TRILOGY MODULAR TRABECULAR METAL 05/31/2017
ZIMMER, INC. UNKNOWN TRILOGY MODULAR TRABECULAR METAL 05/31/2017
ZIMMER, INC. UNKNOWN LONGEVITY HIGHLY CROSS-LINKED PO 05/31/2017
ZIMMER, INC. UNKNOWN ZMR FEMORAL STEM 05/06/2017
BIOMET ORTHOPEDICS UNKNOWN HEAD 03/24/2017
DEPUY ORTHOPAEDICS INC US PINNACLE MTL INS NEUT36IDX52OD 03/14/2017
DEPUY INTERNATIONAL LTD. 8010379 TOTAL ASR FEM IMP SIZE 53 03/10/2017
DEPUY INTERNATIONAL LTD. 8010379 TAPER SLEEVE ADAPTER 12/14 +2 02/21/2017
DEPUY ORTHOPAEDICS INC US PINNACLE MTL INS NEUT36IDX60OD 02/13/2017
DEPUY ORTHOPAEDICS INC US UNKNOWN DEPUY METAL FEMORAL HEAD 01/25/2017
-
-