Core-Nexus
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K131522 | CORE PEDICLE SCREW SYSTEM | MNI | 2013-08-09 | View |
| 510(k) | K131520 | NEXUS ANTERIOR CERVICAL PLATE SYSTEM | KWQ | 2013-07-11 | View |
No matching devices.
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