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
 

 
 
9 records meeting your search criteria returned- Product Code: NTG Patient Problem: Tissue Damage Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
STRYKER GMBH UNKNOWN TIBIAL COMPONENT 03/02/2020
STRYKER GMBH UNKNOWN TALAR COMPONENT 03/02/2020
STRYKER GMBH UNKNOWN STAR ANKLE 11/07/2018
STRYKER GMBH SLIDING CORE UHMPWE, 6MM 04/19/2017
STRYKER GMBH TALAR COMP,SINGLE COATED US VERS MEDIUM, 02/28/2017
STRYKER GMBH TIBIAL COMP,SINGLECOATED US VERS, X-LARG 02/28/2017
STRYKER GMBH SLIDING CORE, UHMPWE,7MM 02/28/2017
STRYKER GMBH STAR TIBIA IMPLANT 05/03/2016
STRYKER GMBH STAR TALAR IMPLANT 05/03/2016
-
-