SeaSpine Orthopedics Corporation
FDA 510(k) & PMA Approved Devices — 67 products
Total Devices67
Categories12
Latest FDA decision2026-07-01
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K170569 | SeaSpine Shoreline ACS - Anterior Cervical Standalone System | OVE | 2017-06-15 | View |
| 510(k) | K163604 | SeaSpine® Daytona® Small Stature Spinal System | NKB | 2017-03-09 | View |
| 510(k) | K162351 | SeaSpine® Vu a•POD™ Prime NanoMetalene® Intervertebral Body Fusion Device | OVD | 2016-12-01 | View |
| 510(k) | K162715 | SeaSpine Spacer System- Hollywood NanoMetalene, Hollywood VI NanoMetalene, Ventura NanoMetalene; SeaSpine Cambria NanoMetalene | MAX | 2016-10-28 | View |
| 510(k) | K161081 | SeaSpine Shoreline ACS - Anterior Cervical Standalone System | OVE | 2016-09-14 | View |
| 510(k) | K161535 | SeaSpine® NewPort™ Spinal System | NKB | 2016-09-08 | View |
| 510(k) | K160902 | Mariner Pedicle Screw System | NKB | 2016-05-26 | View |
No matching devices.
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