• 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
 

 
 
 1 
 2 
 > 
 
18 records meeting your search criteria returned- Product Code: KXA Patient Problem: Joint Disorder Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY INTERNATIONAL LTD - 8010379 9/10 ULTAMET 36MM HEADS +0 04/20/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 03/11/2020
DEPUY IRELAND - 9616671 UNK ATTUNE FEMORAL 01/06/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL HEAD 12/06/2019
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL HEAD 11/27/2019
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 10/24/2019
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL HEAD 10/24/2019
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL AUGMENT 10/07/2019
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 10/07/2019
DEPUY INTERNATIONAL LTD - 8010379 ASR UNI FEMORAL IMPL SIZE 51 11/19/2018
-
-