Spine Wave, Inc.
FDA 510(k) & PMA Approved Dispositivos — 24 products
Publicidad
Total de dispositivos24
Categorías0
Última decisión de la FDA
| Tipo | Número | Nombre del dispositivo | Código | Fecha | Acciones |
|---|---|---|---|---|---|
| 510(k) | K260286 | Dynamo™ Spinal Cement; Salvo® Spine System | PML | 2026-06-15 | Ver |
| 510(k) | K261159 | Exceed® Biplanar Expandable Interbody System | MAX | 2026-05-29 | Ver |
| 510(k) | K243816 | Testa TP Pivoting Spacer System | MAX | 2025-06-27 | Ver |
| 510(k) | K251131 | Annex® 2 Adjacent Level System | NKB | 2025-06-06 | Ver |
| 510(k) | K243514 | Salvo® Robotic Navigation Instruments | OLO | 2025-04-03 | Ver |
| 510(k) | K240685 | Salvo® Spine System | NKB | 2024-05-06 | Ver |
| 510(k) | K231275 | Exceed™ Biplanar Expandable Interbody System | MAX | 2023-07-25 | Ver |
| 510(k) | K222362 | Salvo® Spine System | NKB | 2022-08-29 | Ver |
| 510(k) | K202476 | Salvo® Spine System | NKB | 2020-11-05 | Ver |
| 510(k) | K192526 | Spine Wave Navigated Instruments | OLO | 2019-10-10 | Ver |
| 510(k) | K191045 | Salvo™ Spine System | NKB | 2019-07-10 | Ver |
| 510(k) | K182954 | Salvo™ Spine System | NKB | 2018-12-12 | Ver |
| 510(k) | K181596 | Spine Wave Navigated Instruments | OLO | 2018-10-24 | Ver |
| 510(k) | K181440 | Proficient® Posterior Cervical Spine System | NKG | 2018-07-30 | Ver |
| 510(k) | K172594 | Proficient® Posterior Cervical Spine System | NKG | 2017-12-15 | Ver |
| 510(k) | K173175 | Paramount Anterior Cervical Cage System | OVE | 2017-11-01 | Ver |
| 510(k) | K172175 | CapSure® PS System | NKB | 2017-08-16 | Ver |
| 510(k) | K163246 | Leva Anterior Expandable Spacer System | MAX | 2017-04-06 | Ver |
| 510(k) | K162760 | Spine Wave Anterior Cervical Spine System | OVE | 2017-02-16 | Ver |
| 510(k) | K162639 | Proficient™ Posterior Cervical Spine System | NKG | 2017-02-07 | Ver |
No hay dispositivos coincidentes.