Medical Device Manufacturer · US , Sunnyvale , CA

Avantec Vascular Corp. - FDA 510(k) Cleared Devices

3 submissions · 1 cleared · Since 2003

3

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Avantec Vascular Corp. Gastroenterology & Urology ✕

2 devices

1-2 of 2

Cleared Feb 04, 2004

DURAMAX .018 BILIARY STENT SYSTEM

Gastroenterology & Urology · 181d

Cleared Jul 09, 2003

DURAMAX .035 BILIARY STENT SYSTEM, MODELS DML0718-80, DML0718-135,...

Gastroenterology & Urology · 131d