FDA 510(k) Applications Submitted by MELISSA S MURPHY
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K031068 |
04/04/2003 |
STRYKER VISUM SURGICAL LIGHTING SYSTEM |
Stryker Endoscopy |
| K061063 |
04/17/2006 |
MODIFICATION TO: SILVERHAWK PERIPHERAL PLAQUE EXCISION SYSTEM, MODELS P4028/FG08300 |
FOXHOLLOW TECHNOLOGIES, INC. |
| K041305 |
05/17/2004 |
STRYKER BIOZIP SUTURE ANCHOR SYSTEM |
Stryker Endoscopy |
| K041307 |
05/17/2004 |
MODIFICATION TO STRYKER XCEL ANCHOR SYSTEM |
Stryker Endoscopy |
| K041310 |
05/17/2004 |
STRYKER WEDGE SUTURE ANCHOR SYSTEM |
Stryker Endoscopy |
| K032901 |
09/17/2003 |
STRYKER MINI-MENDER MENISCAL REPAIR SYSTEM |
Stryker Endoscopy |
| K033252 |
10/08/2003 |
MODIFICATION TO STRYKER BIOABSORBABLE INTERFERENCE SCREW SYSTEM |
Stryker Endoscopy |
| 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 |
| K061188 |
04/28/2006 |
SILVERHAWK PERIPHERAL PLAQUE EXCISION SYSTEM |
FOXHOLLOW TECHNOLOGIES, INC. |
| K071432 |
05/23/2007 |
SILVERHAWK-R PERIPHERAL PLAQUE EXCISION SYSTEM FOR SURGICAL USE |
FOX HOLLOW TECHNOLOGIES |
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