Fox Hollow Technologies
Fox Hollow Technologies holds FDA 510(k) medical device clearances, first cleared 2003, most recent 2008.
Top product codes for Fox Hollow Technologies
Recent clearances by Fox Hollow Technologies
- K071432 — SILVERHAWK-R PERIPHERAL PLAQUE EXCISION SYSTEM FOR SURGICAL USE
- K071826 — THE RINSPIRATOR, MODELS FG09770, FG08776, FG08777, FG08910
- K053460 — MODIFICATION TO SILVERHAWK PERIPHERAL PLAQUE EXCISION SYSTEM, MODELS 02550, 04800, 05200, 06002, 02406, 04706, 04300,
- K043553 — SILVERHAWK PERIPHERAL PLAQUE EXCISION SYSTEM, MODELS 02550,04800, 05200, 02406, 04706, 04300
- K024243 — REFORM PERIPHERAL CATHETER SYSTEM, MODEL 02200; REFORM PERIPHERAL CATHETERCATHETER, MODEL 02406
Data sourced from openFDA. This site is unofficial and independent of the FDA.