Orthosensor, Inc.
FDA 510(k) & PMA Approved Dispositivos — 5 products
Publicidade
Total de dispositivos5
Categorias0
Última decisão da FDA
| Tipo | Número | Nome do dispositivo | Código | Data | Ações |
|---|---|---|---|---|---|
| 510(k) | K200587 | VERASENSE for Exactech Equinoxe Size 38 mm, VERASENSE for Exactech Equinoxe Size 42 mm, LinkStation MINI, LinkStation MINI Evaluation Kit, VERASENSE Software Application for Shoulder | ONN | 2020-08-25 | Ver |
| 510(k) | K200665 | VERASENSE for Stryker Triathlon | ONN | 2020-04-12 | Ver |
| 510(k) | K193580 | VERASENSE for Zimmer Biomet Persona CR C-D/3-9 Left, VERASENSE for Zimmer Biomet Persona CR C-D/3-9 Right, VERASENSE for Zimmer Biomet Persona CR E-F/3-11 Left, VERASENSE for Zimmer Biomet Persona CR E-F/3-11 Right, VERASENSE for Zimmer Biomet Persona CR G-H/7-12 Left | ONN | 2020-04-01 | Ver |
| 510(k) | K180459 | VERASENSE for Zimmer Biomet Persona | ONN | 2018-06-07 | Ver |
| 510(k) | K150372 | VERASENSE Knee System | ONN | 2016-04-15 | Ver |
Nenhum dispositivo correspondente.