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
 

 
 
10 records meeting your search criteria returned- Product Code: JDN Patient Problem: Failure of Implant Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CTL MEDICAL CORPORATION TAURUS 11/04/2022
MEDICREA INTERNATIONAL PASS LP 12/07/2020
MEDICREA INTERNATIONAL PASS LP 09/30/2020
MEDOS INTERNATIONAL SàRL CH UNKNOWN OTHER PRODUCTS 01/24/2019
SEASPINE INC. SKIPJACK EXPANDABLE INTERBODY SYSTEM 12/05/2018
SYNTHES USA IMPLANT, FIXATION DEVICE, SPINAL 08/10/2017
NUVASIVE, INC. NUVASIVE HELIX-T ACP SYSTEM 02/18/2015
NUVASIVE, INC. SPHERX DEFORMITY SYSTEM 02/13/2015
SYNTHES (USA) IMPLANT, FIXATION DEVICE, SPINAL 01/30/2015
SYNTHES USA IMPLANT, FIXATION DEVICE, SPINAL 01/09/2015
-
-