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
 

 
 
8 records meeting your search criteria returned- Product Code: HSX Product Problem: Failure to Osseointegrate Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SMITH & NEPHEW, INC. ENGAGE POROUS TIBIAL TRAY SZ 4-RT MED 12/19/2023
SMITH & NEPHEW, INC. ENGAGE POROUS FEMORAL SZ 4-RT MED 04/13/2023
SMITH & NEPHEW, INC. ENGAGE POROUS FEMORAL SZ 2-LT MED 03/13/2023
SMITH & NEPHEW, INC. ENGAGE POROUS TIBIAL TRAY SZ 3-LT MED 02/27/2023
SMITH & NEPHEW, INC. JRNY UNI TIBIAL BASE LM/RL SZ 5 09/08/2022
SMITH & NEPHEW, INC. JRNY UNI TIBIAL BASE LM/RL SZ 3 09/08/2022
SMITH & NEPHEW, INC. JRNY UNI TIBIAL BASE LM/RL SZ 4 09/06/2022
SMITH & NEPHEW, INC. JRNY UNI TIBIAL BASE LM/RL SZ 4 09/05/2022
-
-