Jeil Medical Corporation
FDA 510(k) & PMA Approved Dispositivos — 35 products
Publicidad
Total de dispositivos35
Categorías0
Última decisión de la FDA
| Tipo | Número | Nombre del dispositivo | Código | Fecha | Acciones |
|---|---|---|---|---|---|
| 510(k) | K252246 | Leforte MMF System | JEY | 2026-04-02 | Ver |
| 510(k) | K252826 | ARIX Femur Nail System | HSB | 2025-12-10 | Ver |
| 510(k) | K251431 | FIX-C PEEK ACIF SA System | OVE | 2025-06-27 | Ver |
| 510(k) | K243973 | FIX-L PEEK PLIF and T-PLIF System | MAX | 2025-06-12 | Ver |
| 510(k) | K242751 | Sistema ARIX Pectus Bar | HRS | 2025-05-30 | Ver |
| 510(k) | K242247 | ARIX Femur Nail System | HSB | 2025-04-22 | Ver |
| 510(k) | K243915 | FIX-C 3D Ti ACIF System | ODP | 2025-02-18 | Ver |
| 510(k) | K243004 | Xpine Spinal Fixation System | NKB | 2024-11-08 | Ver |
| 510(k) | K231251 | FlexWing Anterior Cervical Plate System | KWQ | 2024-07-24 | Ver |
| 510(k) | K233912 | ARIX Cannulated Screw System | HWC | 2024-03-11 | Ver |
| 510(k) | K231887 | ARIX Ankle Distal Tibia System | HRS | 2023-12-14 | Ver |
| 510(k) | K231441 | ARIX Ankle System | HRS | 2023-07-17 | Ver |
| 510(k) | K230938 | Sistema ARIX Humerus | HRS | 2023-05-03 | Ver |
| 510(k) | K221412 | Sistema ARIX Rib | HRS | 2022-11-22 | Ver |
| 510(k) | K221920 | Sistema ARIX Small Fragment | HRS | 2022-08-24 | Ver |
| 510(k) | K212266 | FIX-C PEEK Anterior Cervical Interbody System | ODP | 2021-12-21 | Ver |
| 510(k) | K202912 | ARIX Ankle Distal Tibia System | HRS | 2020-10-29 | Ver |
| 510(k) | K201656 | ARIX Elbow System | HRS | 2020-09-15 | Ver |
| 510(k) | K193616 | ARIX Ankle System | HRS | 2020-03-04 | Ver |
| 510(k) | K192417 | ARIX Cannulated Screw System | HWC | 2019-11-26 | Ver |
No hay dispositivos coincidentes.