• 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
 

 
 < 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 16 
 17 
 > 
 
275 records meeting your search criteria returned- Product Code: KWP Product Problem: Material Deformation Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
WARSAW ORTHOPEDICS CD HORIZON SPINAL SYSTEM 12/27/2019
WARSAW ORTHOPEDICS CD HORIZON SPINAL SYSTEM 12/20/2019
WARSAW ORTHOPEDICS CD HORIZON SPINAL SYSTEM 12/08/2019
WARSAW ORTHOPEDICS VERTEX RECONSTRUCTION SYSTEM 12/05/2019
WARSAW ORTHOPEDICS VERTEX RECONSTRUCTION SYSTEM 10/30/2019
MEDTRONIC SOFAMOR DANEK USA, INC. APPLIANCE, FIXATION, SPINAL INTERLAMINAL 10/02/2019
WARSAW ORTHOPEDICS CD HORIZON SOLERA SPINAL SYSTEM 09/18/2019
WARSAW ORTHOPEDICS CD HORIZON SOLERA SPINAL SYSTEM 08/16/2019
ZIMMER BIOMET SPINE INC. POLYAXIAL SCREW (DIA. 4.5 MM X 45 MM L) 06/28/2019
WARSAW ORTHOPEDICS CD HORIZON SPINAL SYSTEM 06/07/2019
-
-