• 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
 

 
 < 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 > 
 
124 records meeting your search criteria returned- Product Code: NJE Product Problem: Break Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
STRYKER NEUROVASCULAR CORK NEUROFORM ATLAS STENT SYSTEM 4.5 X 30MM 08/06/2018
STRYKER NEUROVASCULAR CORK F/G WINGSPAN STENT SYSTEM 4.0 X 20MM 06/22/2018
STRYKER NEUROVASCULAR CORK NEUROFORM ATLAS STENT SYSTEM 3.0 X 24MM 06/13/2018
STRYKER NEUROVASCULAR CORK NEUROFORM ATLAS STENT SYSTEM 4.0 X 21MM 05/14/2018
STRYKER NEUROVASCULAR CORK NEUROFORM 3 EZ- 4.5 X 20MM 05/03/2018
STRYKER NEUROVASCULAR CORK NEUROFORM ATLAS STENT SYSTEM 3.0 X 21MM 05/01/2018
STRYKER NEUROVASCULAR CORK UNKNOWN_NEUROVASCULAR_PRODUCT 04/10/2018
STRYKER NEUROVASCULAR CORK UNKNOWN_NEUROVASCULAR_PRODUCT 04/10/2018
STRYKER NEUROVASCULAR CORK NEUROFORM 3 EZ- 3.0 X 20MM 04/06/2018
STRYKER NEUROVASCULAR-CALIF UNKNOWN_NEUROVASCULAR_PRODUCT 03/13/2018
-
-