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 
 7 
 > 
 
66 records meeting your search criteria returned- Product Code: JDI Patient Problem: Fibrosis Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDIC INC, 1818910 ARTICULEZE M HEAD 36MM -2 02/07/2018
DEPUY ORTHOPAEDICS INC US ARTICULEZE M HEAD 36MM +1.5 01/22/2018
DEPUY INTERNATIONAL LTD - 8010379 ARTICULEZE M HEAD 36MM +1.5 01/03/2018
DEPUY ORTHOPAEDICS INC US LPS PC FEM STEM 11.5X150MM BOW 12/07/2017
DEPUY ORTHOPAEDICS, INC. 1818910 S-ROM M HEAD 36MM+12 NON SKIRT 11/30/2017
DEPUY ORTHOPAEDICS INC US 12/14 ARTICUL 40MM M SPEC+12 07/24/2017
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN PCA CUP 06/02/2017
DEPUY ORTHOPAEDICS INC US AML SM STATURE 15.0MM 05/04/2017
DEPUY ORTHOPAEDICS INC US ARTICULEZE M HEAD 36MM +8.5 05/04/2017
DEPUY ORTHOPAEDICS, INC. 1818910 ARTICULEZE M HEAD 36MM -2 04/04/2017
-
-