FDA 510(k) Applications Submitted by LAETITIA BERNARD
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K020411 |
02/07/2002 |
NUVASIVE TRIAD FACET SCREW SYSTEM |
NUVASIVE, INC. |
| K040543 |
03/02/2004 |
NUVASIVE NEUROVISION JJB SYSTEM |
NUVASIVE, INC. |
| K040657 |
03/12/2004 |
BOUSSIGNAC/VYGON ENDOTRACHEAL TUBE, MODEL 6501.25/30/35 AND 6502.70/75/80 |
VYGON S A |
| K020853 |
03/15/2002 |
NUVASIVE MESH |
NUVASIVE, INC. |
| K001323 |
04/26/2000 |
NUVASIVE PERCUTANEOUS TRANSFACET/INTRAPEDICULAR SCREW |
NUVASIVE, INC. |
| K041447 |
06/01/2004 |
NUVASIVE ANTERIOR CERVICAL PLATE SYSTEM |
NUVASIVE, INC. |
| K032083 |
07/07/2003 |
NUVASIVE NEUROVISION JJB SYSTEM |
NUVASIVE, INC. |
| K032180 |
07/17/2003 |
NUVASIVE CEMENT RESTRICTOR |
NUVASIVE, INC. |
| K032476 |
08/12/2003 |
NUVASIVE MESH |
NUVASIVE, INC. |
| K042449 |
09/09/2004 |
DOLPHIN INFLATION DEVICE |
SEDAT S.A. |
| K013257 |
10/01/2001 |
HEMI-ARC SURGICAL NAVIGATOR |
NUVASIVE, INC. |
| K023319 |
10/04/2002 |
NUVASIVE MASH |
NUVASIVE, INC. |
| K033546 |
11/12/2003 |
NUVASIVE SPINAL SYSTEM |
NUVASIVE, INC. |
| K013884 |
11/23/2001 |
BOUSSIGNAC C.P.A.P. DEVICE |
VYGON S A |
|
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