• 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 
 > 
 
27 records meeting your search criteria returned- Product Code: KWP Product Problem: Device Inoperable Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
GLOBUS ACADIA 01/25/2018
WARSAW ORTHOPEDICS CD HORIZON SPINAL SYSTEM 01/24/2018
WARSAW ORTHOPEDICS CD HORIZON SPINAL SYSTEM 12/22/2017
WARSAW ORTHOPEDICS CD HORIZON SPINAL SYSTEM 10/04/2017
WARSAW ORTHOPEDICS TSRH SPINAL SYSTEM 05/16/2017
WARSAW ORTHOPEDICS CD HORIZON SPINAL SYSTEM 04/06/2017
WARSAW ORTHOPEDICS CD HORIZON SPINAL SYSTEM 09/26/2016
MDT SOFAMOR DANEK PUERTO RICO MFG CD HORIZON SPINAL SYSTEM 09/21/2016
ZIMMER SPINE VIRAGE, TOWER ROD REDUCER 09/01/2016
ZIMMER SPINE VIRAGE TOWER ROD REDUCER 08/03/2016
-
-