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

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 
 3 
 4 
 5 
 
 
49 records meeting your search criteria returned- Product Code: JDI Product Problem: Failure to Osseointegrate Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER, INC. UNKNOWN STEM 05/08/2017
ZIMMER, INC. UNKNOWN ZMR CONE BODY 05/07/2017
ZIMMER, INC. UNKNOWN ZMR FEMORAL STEM 05/07/2017
BIOMET ORTHOPEDICS UNKNOWN ZMR FEMORAL STEM 03/24/2017
BIOMET ORTHOPEDICS UNKNOWN STEM 03/24/2017
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN TRIDENT CUP 11/20/2015
BIOMET ORTHOPEDICS M2A 38MM MOD HD STD NK 01/13/2015
STRYKER ORTHOPAEDICS-MAHWAH SIZE 5 ACCOLADE II 127 DEG 10/28/2014
DEPUY ORTHOPAEDICS, INC. 1818910 PINN MULTIHOLE W/GRIPTION 62MM 01/07/2014
-
-