Atlas Spine, Inc.
FDA 510(k) & PMA Approved Devices — 10 products
Total Devices10
Categories6
Latest FDA decision2026-07-15
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K252822 | Atlas Spine HiRISE™ Expandable Cervical-p Corpectomy Implant | PLR | 2026-07-15 | View |
| 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.