Alphatec Spine
FDA 510(k) & PMA Approved Dispositivos — 6 products
Publicidade
Total de dispositivos6
Categorias0
Última decisão da FDA
| Tipo | Número | Nome do dispositivo | Código | Data | Ações |
|---|---|---|---|---|---|
| 510(k) | K251575 | IdentiTi™ II ALIF Standalone Interbody System; Transcend™ ALIF Standalone Interbody System | OVD | 2025-09-03 | Ver |
| 510(k) | K241375 | IdentiTi Porous Ti Interbody System; IdentiTi NanoTec Interbody System; IdentiTi Cervical Porous Ti Interbody System; IdentiTi NanoTec Cervical Interbody System; IdentiTi Cervical Standalone Interbody System; IdentiTi NanoTec Cervical Standalone Interbody System; IdentiTi ALIF Standalone Interbody System; IdentiTi NanoTec ALIF Standalone Interbody System; Transcend PEEK Interbody System; Transcend NanoTec Interbody System; Transcend Cervical PEEK Interbody System; Transcend NanoTec Cer | MAX | 2025-02-03 | Ver |
| 510(k) | K240951 | Invictus Robotic Navigation Instruments | OLO | 2024-06-06 | Ver |
| 510(k) | K222028 | IdentiTi™ Porous Ti Interbody System, IdentiTi™ NanoTec™ Interbody System, Transcend™ PEEK Interbody System, Transcend™ NanoTec™ Interbody System, IdentiTi™ ALIF Standalone Interbody System, IdentiTi™ NanoTec™ ALIF Standalone Interbody System | MAX | 2022-10-07 | Ver |
| 510(k) | K191185 | Solanas® Posterior OCT Fixation System | NKG | 2019-06-03 | Ver |
| 510(k) | K160958 | Battalion Universal Spacer System | PHM | 2016-09-08 | Ver |
Nenhum dispositivo correspondente.