Atlas Spine, Inc.
FDA 510(k) & PMA Approved Devices — 9 products
Total Devices9
Categories6
Latest Approval2025-11-10
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K252560 | Atlas Spine HiRISE Expandable Cervical Corpectomy System | PLR | 2025-11-10 | View |
| 510(k) | K251969 | Atlas Spine Project X Expandable Posterior Lumbar Interbody System | MAX | 2025-08-15 | View |
| 510(k) | K243191 | Atlas Spine Lateral Expandable Interbody System | OVD | 2024-11-26 | View |
| 510(k) | K202302 | Atlas Spine Rebar (Ti) Spacer System | ODP | 2020-10-30 | View |
| 510(k) | K192570 | Atlas Spine Expandable Cervical Standalone Interbody System | OVE | 2020-02-28 | View |
| 510(k) | K182418 | V3 Segmental Plating System | KWQ | 2018-11-29 | View |
| 510(k) | K180675 | Atlas Spine Expandable Cervical Interbody System | ODP | 2018-06-13 | View |
| 510(k) | K172334 | Ortus Expandable Lumbar Interbody Fusion System | MAX | 2017-10-25 | View |
| 510(k) | K162918 | Atlas Spine Expandable Interbody System | MAX | 2017-02-09 | View |
No matching devices.