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 
 
 
75 records meeting your search criteria returned- Product Code: MAX Product Problem: Detachment of Device or Device Component Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
X-SPINE SYSTEMS, INC. CALIX LUMBAR SPINAL IMPLANT SYSTEM 11/19/2014
ZIMMER SPINE, INC. ARDIS PEEK IMPLANT 13X09X26 08/04/2014
ZIMMER SPINE, INC. ARDIS INSERTER - 9MM 08/04/2014
EBI, LLC ZYSTON INTERBODY SPACER SYSTEMS 07/07/2014
STRYKER SPINE-FRANCE NAVIGATOR STRAIGHT INSERTER 05/06/2014
-
-