Vy Spine, LLC
FDA 510(k) & PMA Approved Devices — 21 products
Total Devices21
Categories8
Latest Approval2026-03-27
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K260697 | VyPlate Anterior Cervical Plate System | KWQ | 2026-03-27 | View |
| 510(k) | K253432 | DiversiVy Facet Screw System | MRW | 2026-03-19 | View |
| 510(k) | K253158 | VyBrate VBR System | MQP | 2026-01-07 | View |
| 510(k) | K241783 | FortiVy OsteoVy Lumbar IBF | MAX | 2025-03-18 | View |
| 510(k) | K242784 | Vy Spine VyLam Laminoplasty System | NQW | 2024-10-16 | View |
| 510(k) | K233807 | LumiVy Lumbar IBF System | MAX | 2024-09-24 | View |
| 510(k) | K231836 | ClariVy Cervical IBF System | ODP | 2023-10-30 | View |
| 510(k) | K231744 | VyLink Spinal Screw System | NKB | 2023-10-13 | View |
| 510(k) | K232471 | Vy Spine VyLam Laminoplasty System | NQW | 2023-10-10 | View |
| 510(k) | K232167 | VySpan PCT System | NKG | 2023-09-27 | View |
| 510(k) | K230414 | ClariVy Cervical IBF System | ODP | 2023-05-12 | View |
| 510(k) | K223513 | UniVy OsteoVy-Ti Cervical IBF System | ODP | 2023-04-18 | View |
| 510(k) | K223852 | VySpan PCT System | NKG | 2023-02-24 | View |
| 510(k) | K223412 | LumiVy Lumbar IBF System | MAX | 2023-01-06 | View |
| 510(k) | K221162 | UniVy OsteoVy Cervical IBF System | ODP | 2022-11-04 | View |
| 510(k) | K221572 | VyPlate Anterior Cervical Plate System | KWQ | 2022-07-26 | View |
| 510(k) | K213750 | VyLink Spinal Screw System | NKB | 2022-02-28 | View |
| 510(k) | K212930 | LumiVy Lumbar IBF System | MAX | 2022-02-16 | View |
| 510(k) | K213219 | Vy Spine VyWasher Buttress System | KWQ | 2021-12-23 | View |
| 510(k) | K212715 | Vy Spine ClariVy Cervical IBF System | ODP | 2021-12-20 | View |
| 510(k) | K213394 | Vy Spine VySpan PCT System | NKG | 2021-12-10 | View |
No matching devices.