FDA 510(k) Applications Submitted by PATRICK BERTRANOU
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K030252 |
01/24/2003 |
ORIA SPINAL CLIP SYSTEM EXTENDED OMNIAXIAL CONNECTORS (CO05 & CO07) |
ORTHOTEC, L.L.C. |
| K010369 |
02/07/2001 |
CLARIS PLATE SYSTEM |
ORTHOTEC, L.L.C. |
| K040346 |
02/12/2004 |
MODIFICATION TO ORIA TOP CLIP SYSTEM |
ORTHOTEC, L.L.C. |
| K030500 |
02/19/2003 |
ORIA ZENITH |
ORTHOTEC, L.L.C. |
| K040514 |
02/27/2004 |
EOVIA CALCIUM PHOSPHATE CERAMIC |
ORTHOTEC, L.L.C. |
| K030958 |
03/27/2003 |
ORIA SPINAL SYSTEM, DOMINO AND TUBE CONNECTORS |
ORTHOTEC, L.L.C. |
| K971453 |
04/21/1997 |
ORTHOTEC K-CAP SYSTEM |
ORTHOTECH |
| K031452 |
05/07/2003 |
ORIA SPINAL CLIP SYSTEM, SACRAL CONNECTOR, MODELS CA03 AND AO03 |
ORTHOTEC, L.L.C. |
| K031471 |
05/09/2003 |
ORIA SPINAL CLIP SYSTEM, LATERAL INTERMEDIATE CONNECTOR, MODEL AL01 |
ORTHOTEC, L.L.C. |
| K021679 |
05/21/2002 |
ORIA SPINAL CLIP SYSTEM |
ORTHOTEC, L.L.C. |
| K023377 |
10/08/2002 |
ORIA CERVICAL PLATES |
ORTHOTEC, L.L.C. |
| K023378 |
10/08/2002 |
ORIA CLARIS |
ORTHOTEC, L.L.C. |
| K023884 |
11/21/2002 |
MODIFICATION ORIA SPINAL SYSTEM |
ORTHOTEC, L.L.C. |
| K023994 |
12/03/2002 |
ORIA SPINAL CLIP SYSTEM, TYPES BD AND BJ |
ORTHOTEC, L.L.C. |
| K003733 |
12/04/2000 |
SCS CLOSED SCREW |
ORTHOTEC, L.L.C. |
| K003823 |
12/11/2000 |
SCS DT-02 TRANSVERSE CONNECTOR |
ORTHOTEC, L.L.C. |
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