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

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 
 > 
 
58 records meeting your search criteria returned- Product Code: KXA Patient Problem: Weakness Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY INTERNATIONAL LTD - 8010379 ASR TAP SLV ADAP 12/14 -1 11/07/2018
DEPUY INTERNATIONAL LTD - 8010379 ADAPTER SLEEVES 12/14 +2 06/18/2018
DEPUY INTERNATIONAL LTD. 8010379 ASR ACETABULAR IMPLANT 52 03/01/2018
DEPUY INTERNATIONAL LTD. 8010379 UNKNOWN HIP FEMORAL AUGMENT 02/16/2018
DEPUY INTERNATIONAL LTD. 8010379 UNKNOWN HIP FEMORAL HEAD 02/16/2018
DEPUY INTERNATIONAL LTD - 8010379 ADAPTER SLEEVES 12/14 +2 02/16/2018
DEPUY INTERNATIONAL LTD - 8010379 ADAPTER SLEEVES 12/14 +5 01/15/2018
DEPUY INT'L LTD. 8010379 UNKNOWN HIP FEMORAL AUGMENT 12/13/2017
DEPUY ORTHOPAEDICS, INC. 1818910 TRI-LOCK BPS SZ 7 HI OFFSET 11/17/2017
DEPUY INTERNATIONAL LTD - 8010379 ASR 300 SPIKED CUP SIZE 60 06/19/2017
-
-