Medical Device Manufacturer · US , Redwood City , CA

Fox Hollow Technologies - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2003

Recent clearances: SILVERHAWK-R PERIPHERAL PLAQUE EXCISION SYSTEM FOR SURGICAL USE, THE RINSPIRATOR, MODELS FG09770, FG08776, FG08777, FG08910, MODIFICATION TO SILVERHAWK PERIPHERAL PLAQUE EXCISION SYSTEM, MODELS 02550, 04800, 05200, 06002, 02406, 04706, 04300,

View 5 510(k) Devices ↓

5

Total

5

Cleared

0

Denied

Fox Hollow Technologies has 5 FDA 510(k) cleared medical devices. Based in Redwood City, US.

Historical record: 5 cleared submissions from 2003 to 2008. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Fox Hollow Technologies Filter by specialty or product code using the sidebar.

Fox Hollow Technologies is one of 21653 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Fox Hollow Technologies

5 devices

1-5 of 5

Cleared Feb 12, 2008

SILVERHAWK-R PERIPHERAL PLAQUE EXCISION SYSTEM FOR SURGICAL USE

Cardiovascular · 265d

Cleared Nov 09, 2007

THE RINSPIRATOR, MODELS FG09770, FG08776, FG08777, FG08910

Cardiovascular · 129d

Cleared Jan 13, 2006

MODIFICATION TO SILVERHAWK PERIPHERAL PLAQUE EXCISION SYSTEM, MODELS 02550,...

Cardiovascular · 31d

Cleared Feb 18, 2005

SILVERHAWK PERIPHERAL PLAQUE EXCISION SYSTEM, MODELS 02550,04800, 05200,...

Cardiovascular · 53d

Cleared Jun 20, 2003

REFORM PERIPHERAL CATHETER SYSTEM, MODEL 02200

Cardiovascular · 179d