• 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 
 > 
 
13 records meeting your search criteria returned- Product Code: NEK Patient Problem: Urinary Frequency 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 10/14/2015
MEDTRONIC SOFAMOR DANEK USA, INC INFUSE BONE GRAFT 10/08/2015
MEDTRONIC SOFAMOR DANEK USA, INC INFUSE BONE GRAFT 09/15/2015
MEDTRONIC SOFAMOR DANEK USA, INC INFUSE BONE GRAFT 02/04/2015
MEDTRONIC SOFAMOR DANEK USA, INC INFUSE BONE GRAFT 01/30/2015
MEDTRONIC SOFAMOR DANEK USA, INC INFUSE BONE GRAFT 12/26/2014
MEDTRONIC SOFAMOR DANEK USA, INC INFUSE BONE GRAFT 11/07/2014
MEDTRONIC SOFAMOR DANEK USA, INC INFUSE BONE GRAFT 11/03/2014
MEDTRONIC SOFAMOR DANEK USA, INC INFUSE BONE GRAFT 10/27/2014
MEDTRONIC SOFAMOR DANEK USA, INC INFUSE BONE GRAFT 06/26/2014
-
-