Spine Wave, Inc.
FDA 510(k) & PMA Approved Devices — 24 products
Total Devices24
Categories8
Latest FDA decision2026-06-15
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K161993 | Leva® Anterior Interbody System | OVD | 2016-11-22 | View |
| 510(k) | K153222 | Leva Spacer System | MAX | 2016-04-15 | View |
| 510(k) | K160003 | Sniper (R) Spine System | MNI | 2016-02-26 | View |
| 510(k) | K152620 | Spine Wave Gen II Expandable Interbody System | MAX | 2016-01-15 | View |
No matching devices.
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