FDA 510(k) Applications Submitted by FOXHOLLOW TECHNOLOGIES, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K061063 | 04/17/2006 | MODIFICATION TO: SILVERHAWK PERIPHERAL PLAQUE EXCISION SYSTEM, MODELS P4028/FG08300 | FOXHOLLOW TECHNOLOGIES, INC. |
| K061188 | 04/28/2006 | SILVERHAWK PERIPHERAL PLAQUE EXCISION SYSTEM | FOXHOLLOW TECHNOLOGIES, INC. |
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