# Medtronic Percusurge, Inc.

- Location (FDA's records): Sunnyvale, CA
- FDA decisions: 2 (2002–2002): 2 510(k) clearances
- Product codes: NFA (2)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 8 (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 that cite its devices most
- Medtronic Vascular: 2 (https://510kreport.com/company/medtronic-vascular)
- Kensey Nash Corp.: 1 (https://510kreport.com/company/kensey-nash)
- Boston Scientific Corp: 1 (https://510kreport.com/company/boston-scientific)
- Velocimed, Inc.: 1 (https://510kreport.com/company/velocimed)
- Medtronic, Inc.: 1 (https://510kreport.com/company/medtronic)
- Boston Scientific Epi: 1 (https://510kreport.com/company/boston-scientific-epi)
- St Jude Medical: 1 (https://510kreport.com/company/st-jude-medical)

## Its most-cited devices
- K013913: Percusurge Guardwire Plus Temporary Occlusion and Aspiration System (2002), cited by 6
- K014223: Modification to Guardwire Plus Temporary Occlusion & Aspiration System (2002), cited by 2

## Recent decisions
- K013913: Percusurge Guardwire Plus Temporary Occlusion and Aspiration System (Nov 15, 2002)
- K014223: Modification to Guardwire Plus Temporary Occlusion & Aspiration System (Jan 25, 2002)

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