Medical Device Manufacturer · US , Redwood City , CA

Foxhollow Technologies, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2006

Recent clearances: SILVERHAWK PERIPHERAL PLAQUE EXCISION SYSTEM, MODIFICATION TO: SILVERHAWK PERIPHERAL PLAQUE EXCISION SYSTEM, MODELS P4028/FG08300

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Foxhollow Technologies, Inc. Cardiovascular ✕

2 devices

1-2 of 2

Cleared Oct 23, 2006

SILVERHAWK PERIPHERAL PLAQUE EXCISION SYSTEM

Cardiovascular · 178d

Cleared May 18, 2006

MODIFICATION TO: SILVERHAWK PERIPHERAL PLAQUE EXCISION SYSTEM, MODELS...

Cardiovascular · 31d