Orthomatrix, Inc.
FDA 510(k) & PMA Approved Devices — 8 products
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Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K010738 | CANNULATED PLUS SCREW SYSTEM | HWC | 2001-08-01 | View |
| 510(k) | K001254 | ORTHOMATRIX, INC. CERCLAGE SYSTEM | JDQ | 2000-12-13 | View |
| 510(k) | K992850 | MAGELLAN TIBIAL INTRAMEDULLARY NAIL | HSB | 2000-03-10 | View |
| 510(k) | K992856 | MAGELLAN HUMERAL INTRAMEDULLARY NAIL | HSB | 2000-03-10 | View |
| 510(k) | K852766 | HA-1000 & HA-500 HYDROXYLAPATITE TOOTH ROOT SUBSTI | LYC | 1985-10-21 | View |
| 510(k) | K852765 | HA-2000 HYDROXYLAPATITE | LYC | 1985-09-23 | View |
| 510(k) | K851367 | HA-1000 & HA-500 HYDROXYLAPATITE-MODIFICATION | DZE | 1985-05-21 | View |
| 510(k) | K842163 | RIDGEMATRIX 20/40 MESH, PERIOMATRIX | LYC | 1984-08-09 | View |
No matching devices.
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