FDA 510(k) Applications Submitted by KERRI DIMARTINO
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K081418 |
05/20/2008 |
SPINAL ELEMENTS BUTTRESS PLATE SYSTEM |
SPINAL ELEMENTS, INC. |
| K091587 |
06/02/2009 |
MERCURY SPINAL SYSTEM |
SPINAL ELEMENTS, INC. |
| K081711 |
06/17/2008 |
LUCENT MAGNUM+ |
SPINAL ELEMENTS, INC. |
| K071724 |
06/25/2007 |
LUCENT |
SPINAL ELEMENTS, INC. |
| K071833 |
07/03/2007 |
MOSAIC DEVICES |
SPINAL ELEMENTS, INC. |
| K081968 |
07/10/2008 |
MODIFICATION TO LUCENT |
SPINAL ELEMENTS, INC. |
| K071914 |
07/11/2007 |
MERCURY SPINAL SYSTEM |
SPINAL ELEMENTS, INC. |
| K062004 |
07/17/2006 |
MODIFICATION TO QUANTUM VERTEBRAL BODY REPLACEMENT |
QUANTUM ORTHOPEDICS, INC. |
| K082353 |
08/15/2008 |
MERCURY SPINAL SYSTEM |
SPINAL ELEMENTS, INC. |
| K082992 |
10/07/2008 |
AXXION LIGHT GUIDE |
SPINAL ELEMENTS, INC. |
| K083230 |
11/03/2008 |
MERCURY SPINAL SYSTEM |
SPINAL ELEMENTS, INC. |
| K083475 |
11/24/2008 |
LUCENT MAGNUM |
SPINAL ELEMENTS, INC. |
| K073348 |
11/29/2007 |
LUCENT MAGNUM |
SPINAL ELEMENTS, INC. |
| K073351 |
11/29/2007 |
CRYSTAL |
SPINAL ELEMENTS, INC. |
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