Aegis Spine
FDA 510(k) & PMA Approved Devices — 1 products
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Total Devices1
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K210035 | ZESPIN SI Joint Fusion System, MegaCerfix Posterior Cervical Fixation System, MegaCerfix Anterior Cervical Plate System, Spinema Lumbar Plate System | OUR | 2021-02-16 | View |
No matching devices.
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