Avantec Vascular Corp

FDA Filings

This page includes the latest FDA filings for Avantec Vascular Corp. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)

• Registration Number: 3003524171
• FEI Number: 3003524171
• Name: AVANTEC VASCULAR CORP.
• Owner & Operator: AVANTEC VASCULAR CORP.
• Contact Address: 870 HERMOSA AVENUE --; Sunnyvale CA 94085 US
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 870 Hermosa Avenue ; SUNNYVALE, CA 94085 US
• Establishment Type:
  • Manufacture Device in the United States for Export Only
  • Manufacture Medical Device

FDA Filings

Device Company	Device	Date
GUDID B342CAP14120 Avantec Vascular Corporation	Captus Vascular Retrieval System	2021-07-21
PMN K170987 | MMX AVANTEC VASCULAR CORP.	Captus	2017-12-30
PMN K170987 Avantec Vascular Corporation	Captus Vascular Retrieval System	2017-08-28
HCG AVANTEC VASCULAR CORP.	IMPAXn	2015-11-17