FDA 510(k) Applications Submitted by VERTEBRON, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K040003 |
01/02/2004 |
VERTEBRON SCP CERVICAL PLATE SYSTEM |
VERTEBRON, INC. |
K033352 |
10/20/2003 |
VERTEBRON PSS PEDICLE SCREW SYSTEM |
VERTEBRON, INC. |
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. |
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. |
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