Spinecraft, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K092825 | APEX SPINE SYSTEM 5.50 MM TITANIUM ROD & POLYAXIAL SCREW WASHER | KWP | 2010-03-16 | View |
| 510(k) | K062513 | APEX SPINE SYSTEM | KWP | 2006-12-22 | View |
| 510(k) | K062496 | OSTEOPORE TCP | MQV | 2006-10-19 | View |
No matching devices.
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