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
 

 
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 > 
 
56 records meeting your search criteria returned- Product Code: NIM Patient Problem: Thrombosis Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SILK ROAD MEDICAL, INC ENROUTE TRANSCAROTID STENT SYSTEM 09/10/2019
SILK ROAD MEDICAL, INC ENROUTE TRANSCAROTID STENT SYSTEM 09/10/2019
SILK ROAD MEDICAL, INC ENROUTE TRANSCAROTID STENT SYSTEM 08/16/2019
SILK ROAD MEDICAL, INC ENROUTE TRANSCAROTID STENT SYSTEM 08/16/2019
SILK ROAD MEDICAL, INC. ENROUTE TRANSCAROTID STENT SYSTEM 06/10/2019
AV-TEMECULA-CT XACT CAROTID STENT SYSTEM 05/10/2019
SILK ROAD MEIDCAL ENROUTE TRANSCAROTID STENT SYSTEM 03/14/2019
AV-TEMECULA-CT XACT CAROTID STENT SYSTEM 03/11/2019
AV-TEMECULA-CT XACT CAROTID STENT SYSTEM 03/11/2019
AV-TEMECULA-CT XACT CAROTID STENT SYSTEM 03/11/2019
-
-