Summit Spine
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2017-06-20
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K163494 | Summit Spine Channel Cervical Interbody Fusion System | ODP | 2017-06-20 | View |
| 510(k) | K170572 | Summit Spine Yellowstone Lumbar Interbody Fusion System | MAX | 2017-04-26 | View |
No matching devices.