Spine Wave, Inc.
FDA 510(k) & PMA Approved Produkte — 24 products
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Produkte insgesamt24
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Neueste FDA-Entscheidung
| Typ | Nummer | Produktname | Code | Datum | Aktionen |
|---|---|---|---|---|---|
| 510(k) | K260286 | Dynamo™ Spinal Cement; Salvo® Spine System | PML | 2026-06-15 | Anzeigen |
| 510(k) | K261159 | Exceed® Biplanar Expandable Interbody System | MAX | 2026-05-29 | Anzeigen |
| 510(k) | K243816 | Testa TP Pivoting Spacer System | MAX | 2025-06-27 | Anzeigen |
| 510(k) | K251131 | Annex® 2 Adjacent Level System | NKB | 2025-06-06 | Anzeigen |
| 510(k) | K243514 | Salvo® Robotic Navigation Instruments | OLO | 2025-04-03 | Anzeigen |
| 510(k) | K240685 | Salvo® Spine System | NKB | 2024-05-06 | Anzeigen |
| 510(k) | K231275 | Exceed™ Biplanar Expandable Interbody System | MAX | 2023-07-25 | Anzeigen |
| 510(k) | K222362 | Salvo® Spine System | NKB | 2022-08-29 | Anzeigen |
| 510(k) | K202476 | Salvo® Spine System | NKB | 2020-11-05 | Anzeigen |
| 510(k) | K192526 | Spine Wave Navigated Instruments | OLO | 2019-10-10 | Anzeigen |
| 510(k) | K191045 | Salvo™ Spine System | NKB | 2019-07-10 | Anzeigen |
| 510(k) | K182954 | Salvo™ Spine System | NKB | 2018-12-12 | Anzeigen |
| 510(k) | K181596 | Spine Wave Navigated Instruments | OLO | 2018-10-24 | Anzeigen |
| 510(k) | K181440 | Proficient® Posterior Cervical Spine System | NKG | 2018-07-30 | Anzeigen |
| 510(k) | K172594 | Proficient® Posterior Cervical Spine System | NKG | 2017-12-15 | Anzeigen |
| 510(k) | K173175 | Paramount Anterior Cervical Cage System | OVE | 2017-11-01 | Anzeigen |
| 510(k) | K172175 | CapSure® PS System | NKB | 2017-08-16 | Anzeigen |
| 510(k) | K163246 | Leva Anterior Expandable Spacer System | MAX | 2017-04-06 | Anzeigen |
| 510(k) | K162760 | Spine Wave Anterior Cervical Spine System | OVE | 2017-02-16 | Anzeigen |
| 510(k) | K162639 | Proficient™ Posterior Cervical Spine System | NKG | 2017-02-07 | Anzeigen |
Keine passenden Geräte.