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

Manufacturer and User Facility Device Experience (MAUDE)
  • 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
 

 
 < 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 > 
 
484 records meeting your search criteria returned- Product Code: KWY Patient Problem: Injury Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS, INC. 1818910 UNKNOWN HIP FEMORAL HEAD 06/28/2019
DEPUY ORTHOPAEDICS, INC. 1818910 UNKNOWN HIP FEMORAL HEAD 06/27/2019
DEPUY ORTHOPAEDICS, INC. 1818910 UNKNOWN HIP ACETABULAR CUP 06/18/2019
DEPUY ORTHOPAEDICS, INC. 1818910 UNKNOWN HIP FEMORAL STEM 06/13/2019
DEPUY ORTHOPAEDICS, INC. 1818910 UNKNOWN HIP FEMORAL STEM 06/11/2019
SMITH & NEPHEW ORTHOPAEDICS AG SL-PLUS STANDARD STEM 3 NON-CEMENTED 06/05/2019
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN_32 10° LINER 06/04/2019
SMITH & NEPHEW ORTHOPAEDICS LTD HEMI HEAD 48MM 05/28/2019
SMITH & NEPHEW ORTHOPAEDICS LTD HEMI HEAD 50MM 05/22/2019
DEPUY ORTHOPAEDICS, INC. 1818910 UNKNOWN HIP ACETABULAR LINERS 05/21/2019
-
-