Orthomatrix, Inc.
8 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| CANNULATED PLUS SCREW SYSTEM (K010738) | Orthomatrix, Inc. | 2001-08-01 |
| ORTHOMATRIX, INC. CERCLAGE SYSTEM (K001254) | Orthomatrix, Inc. | 2000-12-13 |
| MAGELLAN TIBIAL INTRAMEDULLARY NAIL (K992850) | Orthomatrix, Inc. | 2000-03-10 |
| MAGELLAN HUMERAL INTRAMEDULLARY NAIL (K992856) | Orthomatrix, Inc. | 2000-03-10 |
| HA-1000 & HA-500 HYDROXYLAPATITE TOOTH ROOT SUBSTI (K852766) | Orthomatrix, Inc. | 1985-10-21 |
| HA-2000 HYDROXYLAPATITE (K852765) | Orthomatrix, Inc. | 1985-09-23 |
| HA-1000 & HA-500 HYDROXYLAPATITE-MODIFICATION (K851367) | Orthomatrix, Inc. | 1985-05-21 |
| RIDGEMATRIX 20/40 MESH, PERIOMATRIX (K842163) | Orthomatrix, Inc. | 1984-08-09 |
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