# Medtronic Endovascular Innovations

- Location (FDA's records): Santa Rosa, CA
- FDA decisions: 1 (2005–2005): 1 510(k) clearance
- Product codes: DQY (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Cook, Inc.: 2 (https://510kreport.com/company/cook)
- Guidant Cardiac and Vascular Surgery: 1 (https://510kreport.com/company/guidant-cardiac-and-vascular-surgery)

## Firms that cite its devices most
- LeMaitre Vascular, Inc.: 1 (https://510kreport.com/company/lemaitre-vascular)
- Via Biomedical, Inc.: 1 (https://510kreport.com/company/via-biomedical)
- W. L. Gore & Associates, Inc.: 1 (https://510kreport.com/company/w-l-gore-associates)

## Its most-cited devices
- K050038: Reliant Stent Graft Balloon Catheter (2005), cited by 3

## Recent decisions
- K050038: Reliant Stent Graft Balloon Catheter (Apr 13, 2005)

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