FDA 510(k) Applications Submitted by LUIS NESPRIDO
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K000009 |
01/03/2000 |
SPIRAL RADIUS RODDING SYSTEM |
UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC |
| K071376 |
05/17/2007 |
MODIFICATION TO VERTEBRON PSS PEDICLE SCREW SYSTEM |
VERTEBRON, INC. |
| K081567 |
06/04/2008 |
VERTEBRON SSP CERVICAL PLATING SYSTEM |
VERTEBRON, INC. |
| K081597 |
06/06/2008 |
MODIFICATION TO VERTEBRON PSS PEDICLE SCREW SYSTEM |
VERTEBRON, INC. |
| K051716 |
06/27/2005 |
VERTEBRON PSS PEDICLE SCREW SYSTEM |
VERTEBRON, INC. |
| K051815 |
07/05/2005 |
MODIFICATION TO VERTEBRON SCP CERVICAL PLATE SYSTEM |
VERTEBRON, INC. |
| K062110 |
07/24/2006 |
VERTEBRON SCP CERVICAL PLATE SYSTEM |
VERTEBRON, INC. |
| K992784 |
08/19/1999 |
NEXT GENERATION RODDING SYSTEM |
UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC |
| K043152 |
11/15/2004 |
VERTEBRON PSS PEDICLE SCREW SYSTEM |
VERTEBRON, INC. |
| K043181 |
11/17/2004 |
MODIFICATION TO VERTEBRON SCP CERVICAL PLATE SYSTEM |
VERTEBRON, INC. |
| K073502 |
12/13/2007 |
VERTEBRON VBR SYSTEM |
VERTEBRON, INC. |
|
|
