• 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 
 > 
 
164 records meeting your search criteria returned- Product Code: MAX Product Problem: Material Integrity Problem Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC NAVIGATION, INC PERCUTANEOUS REFERENCE CROSS PIN FRAME 07/02/2019
AURORA SPINE INC VOX LLIF INTERBODY SYSTEM 06/27/2019
AURORA SPINE INC EOS TLIF INTERBODY SYSTEM 06/26/2019
MEDTRONIC NAVIGATION, INC unknown brand name 06/20/2019
MEDTRONIC NAVIGATION, INC INST 9730605 FRAME REF SM PASSIVE SP 06/11/2019
MEDTRONIC NAVIGATION, INC FRAME REF SM PASSIVE SP 05/24/2019
AESCULAP AG TSPACE PEEK IMPLANT 5° 26X11.5X9MM 05/08/2019
STRYKER SPINE-US 9MM X 6DEG X11MM X 28MM 04/26/2019
MEDTRONIC NAVIGATION, INC PERCUTANEOUS REFERENCE CROSS PIN FRAME 04/24/2019
MEDTRONIC NAVIGATION, INC PERC REF CROSS PIN FRAME 04/11/2019
-
-