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
 

 
 < 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 > 
 
150 records meeting your search criteria returned- Product Code: KXA Patient Problem: No Consequences Or Impact To Patient Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS INC US S-ROM*NECK TRIAL 36+8MM LATERL 02/11/2020
DEPUY ORTHOPAEDICS INC US UNK FEMORAL TRIAL 02/11/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 01/30/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 01/27/2020
DEPUY ORTHOPAEDICS INC US UNK FEMORAL TRIAL 01/24/2020
DEPUY IRELAND - 9616671 ATTUNE REV FEM CTT TRL SZ 4 R 01/24/2020
DEPUY ORTHOPAEDICS INC US UNK FEMORAL TRIAL 01/21/2020
DEPUY ORTHOPAEDICS INC US UNK FEMORAL TRIAL 01/21/2020
DEPUY ORTHOPAEDICS INC US PFC*SIGMA C/S(PS)BOX TRIAL SZ4 01/15/2020
BIOMET FRANCE S.A.R.L. EXCEPTION 01/15/2020
-
-