Medtronic Vascular - FDA 510(k) Cleared Devices
Recent clearances: Steerant™ Super Stiff Guidewire, 6F Sherpa NX Balanced Guide Catheter, 7F Sherpa NX Balanced Guide Catheter, 5F Launcher Guide Catheter, 6F Launcher Guide Catheter, 7F Launcher Guide Catheter, 8F Launcher Guide Catheter
475
Total
453
Cleared
0
Denied
FDA 510(k) Regulatory Record - Medtronic Vascular Gastroenterology & Urology ✕
3 devices
Cleared
Nov 08, 2007
COMPLETE SE SELF EXPANDING BILIARY STENT SYSTEM
Gastroenterology & Urology
461d
Cleared
Nov 17, 2005
TUNA SYSTEM, MODELS 8909, 8929, 8930, 8934
Gastroenterology & Urology
76d
Cleared
Oct 09, 2003
MEDTRONIC SINGLE USE ESOPHAGEAL MANOMETRIC CATHETER, MEDTRONIC SINGLE USE...
Gastroenterology & Urology
90d