FDA 510(k) Applications Submitted by FOX HOLLOW TECHNOLOGIES
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K053460 |
12/13/2005 |
MODIFICATION TO SILVERHAWK PERIPHERAL PLAQUE EXCISION SYSTEM, MODELS 02550, 04800, 05200, 06002, 02406, 04706, 04300, |
FOX HOLLOW TECHNOLOGIES |
| K043553 |
12/27/2004 |
SILVERHAWK PERIPHERAL PLAQUE EXCISION SYSTEM, MODELS 02550,04800, 05200, 02406, 04706, 04300 |
FOX HOLLOW TECHNOLOGIES |
| K071432 |
05/23/2007 |
SILVERHAWK-R PERIPHERAL PLAQUE EXCISION SYSTEM FOR SURGICAL USE |
FOX HOLLOW TECHNOLOGIES |
| K071826 |
07/03/2007 |
THE RINSPIRATOR, MODELS FG09770, FG08776, FG08777, FG08910 |
FOX HOLLOW TECHNOLOGIES |
| K024243 |
12/23/2002 |
REFORM PERIPHERAL CATHETER SYSTEM, MODEL 02200; REFORM PERIPHERAL CATHETERCATHETER, MODEL 02406 |
FOX HOLLOW TECHNOLOGIES |
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