• 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 
 6 
 7 
 8 
 9 
 10 
 > 
 
139 records meeting your search criteria returned- Product Code: KWY Patient Problem: Inadequate Osseointegration Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SMITH & NEPHEW ORTHOPAEDICS AG SL-PLUS STANDARD STEM 5 NON-CEMENTED 04/16/2022
SMITH & NEPHEW ORTHOPAEDICS AG SL-PLUS STANDARD STEM 2 NON-CEMENTED 04/12/2022
SMITH & NEPHEW ORTHOPAEDICS AG SL-PLUS STANDARD STEM 4 NON-CEMENTED 04/12/2022
SMITH & NEPHEW ORTHOPAEDICS AG SL-PLUS STANDARD STEM 5 NON-CEMENTED 04/12/2022
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP IMPLANT 03/04/2022
DEPUY ORTHOPAEDICS INC US UNKNOWN KNEE IMPLANT 01/14/2022
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP IMPLANT 12/28/2021
SMITH & NEPHEW ORTHOPAEDICS AG UNKN. SL-PLUS FAMILY STEM (UNKN. SUB-FAM 06/14/2021
ZIMMER TMT UNK TMARS SHELL 04/29/2021
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP ACETABULAR CUP 12/29/2020
-
-