• 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 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 ORTHOPAEDICS AG SL-PLUS MIA STEM 3 NON-CEM 11/30/2023
SMITH & NEPHEW ORTHOPAEDICS AG POLARSTEM STEM STD TI/HA 4 NON-CEM 01/18/2023
SMITH & NEPHEW ORTHOPAEDICS AG POLARSTEM STEM LAT.TI/HA 1 NON-CEM 01/18/2023
SMITH & NEPHEW ORTHOPAEDICS AG UNKN. POLARCUP SHELL NON-CEMENTED (TI-PL 07/22/2022
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP ACETABULAR CUP 11/26/2019
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 01/23/2019
DEPUY FRANCE SAS - 3003895575 CORAIL2 LAT COXA VARA SIZE 9 01/11/2019
DEPUY ORTHOPAEDICS, INC. 1818910  UNKNOWN HIP ACETABULAR CUP 10/24/2018
DEPUY ORTHOPAEDICS, INC. 1818910 UNKNOWN HIP ACETABULAR CUP 10/17/2018
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 10/11/2018
-
-