• 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
 

 
 
10 records meeting your search criteria returned- Product Code: KWY Patient Problem: Fibrosis Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS INC US LPS CEM FEM STEM 13X150MM BOW 07/15/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL HEAD 07/10/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL HEAD 01/13/2020
DEPUY INTERNATIONAL LTD - 8010379 UNKNOWN HIP FEMORAL HEAD 11/27/2019
DEPUY ORTHOPAEDICS, INC. 1818910 UNKNOWN HIP FEMORAL STEM 07/19/2019
DEPUY INTERNATIONAL LTD. 8010379 DEPUY ASR XL FEM IMP SIZE 46 07/19/2019
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 06/10/2019
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL HEAD 06/10/2019
DEPUY INTERNATIONAL LTD. 8010379 UNKNOWN HIP FEMORAL HEAD 11/01/2018
DEPUY ORTHOPAEDICS INC US UNKNOWN DEPUY PINNACLE METAL LINER 03/11/2017
-
-