• 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: NEK Patient Problem: Wound Dehiscence Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC SOFAMOR DANEK USA, INC INFUSE BONE GRAFT 02/15/2024
MEDTRONIC SOFAMOR DANEK USA, INC INFUSE® BONE GRAFT 12/06/2021
MEDTRONIC SOFAMOR DANEK USA, INC. INFUSE BONE GRAFT 11/26/2021
MEDTRONIC SOFAMOR DANEK USA, INC INFUSE BONE GRAFT 10/21/2020
MEDTRONIC SOFAMOR DANEK USA, INC FILLER, RECOMBINANT HUMAN BONE MORPHOGEN 09/30/2020
MEDTRONIC SOFAMOR DANEK USA, INC INFUSE BONE GRAFT 04/14/2017
MEDTRONIC SOFAMOR DANEK USA, INC INFUSE BONE GRAFT 11/18/2016
MEDTRONIC SOFAMOR DANEK USA, INC INFUSE BONE GRAFT 08/12/2016
MEDTRONIC SOFAMOR DANEK USA, INC INFUSE BONE GRAFT 07/18/2016
MEDTRONIC SOFAMOR DANEK USA, INC INFUSE BONE GRAFT 05/11/2016
-
-