# Medtronic Ave, Inc.

- Location (FDA's records): Santa Rosa, CA
- FDA decisions: 13 (1999–2003): 13 510(k) clearances
- Product codes: FGE (11), MJN (1), DQX (1)
- Predicates its devices cite: 15 (9 its own); citations of its devices by later devices: 13 (9 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Peripheral Ave: 4 (https://510kreport.com/company/peripheral-ave)
- Micro Therapeutics, Inc.: 2 (https://510kreport.com/company/micro-therapeutics)

## Firms that cite its devices most
- Cook, Inc.: 2 (https://510kreport.com/company/cook)
- Invatec S.P.A.: 1 (https://510kreport.com/company/invatec)
- Cordis Corp.: 1 (https://510kreport.com/company/cordis)

## Its most-cited devices
- K011080: Bridge SE Self-Expanding Stent Delivery System (2001), cited by 3
- K011817: Bridge FX (2001), cited by 3
- K992569: Medtronic Ave Bridge Stent (1999), cited by 1
- K993145: Medtronic Ave Bridge Stent (1999), cited by 1
- K014205: Modification to Bridge Self-Expanding Biliary Stent Delivery System (Bridge SE) (2002), cited by 1
- K030633: Medtronic Ave Bridge Constant Biliary Stent System or ('Constant (2003), cited by 1

## Recent decisions
- K032768: Medtronic, Inc. Racer Biliary Stent System (Racer), Model XD#YF (L) (Oct 9, 2003)
- K030633: Medtronic Ave Bridge Constant Biliary Stent System or ('Constant (Sep 2, 2003)
- K030839: Medtronic Ave Bridge Aurora Biliary Stent System (Aurora) (May 30, 2003)
- K022026: Medtronic Ave Bridge Polaris Biliary Stent System (Polaris) (Jul 19, 2002)
- K014205: Modification to Bridge Self-Expanding Biliary Stent Delivery System (Bridge SE) (Jan 14, 2002)
- K011080: Bridge SE Self-Expanding Stent Delivery System (Oct 11, 2001)
- K011817: Bridge FX (Aug 22, 2001)
- K002346: Wire, Guide, Catheter, Model QSW1000 (Sep 27, 2000)

Source page: https://510kreport.com/company/medtronic-ave