Eminent Spine
FDA 510(k) & PMA Approved Devices — 9 products
Advertisement
Total Devices9
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K250894 | Eminent Spine Posterior SI System | OUR | 2025-10-07 | View |
| 510(k) | K241663 | Eminent Spine 3D Titanium Pedicle Screw System | NKB | 2025-04-28 | View |
| 510(k) | K242069 | Eminent Spine Scoliosis Deformity Pedicle Screw System | NKB | 2024-09-03 | View |
| 510(k) | K212701 | Eminent Spine 3D Cervical Interbody Fusion System | ODP | 2023-02-06 | View |
| 510(k) | K221936 | Standalone ALIF Interbody Fusion System | OVD | 2022-10-17 | View |
| 510(k) | K103068 | KING COBRA ANTERIOR CERVICAL PLATE | KWQ | 2011-01-14 | View |
| 510(k) | K100377 | DIAMONDBACK SPINAL SYSTEM | MNI | 2010-04-22 | View |
| 510(k) | K090415 | EMINENT SPINE BUTTRESS (FANG) PLATE SYSTEM | KWQ | 2009-06-01 | View |
| 510(k) | K090064 | EMINENT SPINE INTERBODY FUSION SYSTEM | MAX | 2009-04-09 | View |
No matching devices.
Advertisement