Fox Hollow Technologies
FDA 510(k) medical device clearances.
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.