Fox Hollow Technologies is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Fox Hollow Technologies - FDA 510(k) Cleared 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.
FDA 510(k) Regulatory Record - Fox Hollow Technologies
5 devices
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