Met One Technologies, LLC
FDA 510(k) & PMA Approved Devices — 4 products
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Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K251732 | Wrist Fracture System | HRS | 2026-02-12 | View |
| 510(k) | K250866 | Sovereign Posterior Cervical System | NKG | 2025-05-20 | View |
| 510(k) | K230851 | Kodiak Lumbar Spacer System | MAX | 2023-05-26 | View |
| 510(k) | K222806 | Kodiak C Spinal Implant System | ODP | 2022-12-22 | View |
No matching devices.
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