• 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 
 > 
 
12 records meeting your search criteria returned- Product Code: KXA Patient Problem: Muscular Rigidity Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS INC US UNKNOWN KNEE FEMORAL STEM 02/21/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 11/14/2019
DEPUY INTERNATIONAL LTD - 8010379 UNKNOWN HIP FEMORAL HEAD 11/14/2019
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 09/19/2019
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 ORTHOPAEDICS INC US ARTICULEZE M HEAD 36MM +1.5 01/20/2016
DEPUY ORTHOPAEDICS, INC. 1818910 SUMMIT POR TAPER SZ7 STD OFF 01/14/2016
DEPUY INTERNATIONAL LTD - 8010379 DEPUY ASR FEM IMPLANT SZ 49 03/26/2015
DEPUY INTERNATIONAL LTD. 8010379 DEPUY ASR XL FEM IMP SIZE 53 12/22/2014
-
-