# Foxhollow Technologies, Inc.

- Location (FDA's records): Redwood City, CA
- FDA decisions: 2 (2006–2006): 2 510(k) clearances
- Product codes: MCW (2)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 10 (0 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
- Fox Hollow Technologies: 2 (https://510kreport.com/company/fox-hollow-technologies)

## Firms that cite its devices most
- Pathway Medical Technologies, Inc.: 2 (https://510kreport.com/company/pathway-medical-technologies)
- Ev3, Inc.: 2 (https://510kreport.com/company/ev3)
- Atheromed, Inc.: 2 (https://510kreport.com/company/atheromed)
- Medtronic Vascular: 2 (https://510kreport.com/company/medtronic-vascular)
- Avinger, Inc.: 1 (https://510kreport.com/company/avinger)
- Fox Hollow Technologies: 1 (https://510kreport.com/company/fox-hollow-technologies)

## Its most-cited devices
- K061188: Silverhawk Peripheral Plaque Excision System (2006), cited by 7
- K061063: Modification to: Silverhawk Peripheral Plaque Excision System, Models P4028/FG08300 (2006), cited by 3

## Recent decisions
- K061188: Silverhawk Peripheral Plaque Excision System (Oct 23, 2006)
- K061063: Modification to: Silverhawk Peripheral Plaque Excision System, Models P4028/FG08300 (May 18, 2006)

Source page: https://510kreport.com/company/foxhollow-technologies