Tdm Co., Ltd.
FDA 510(k) & PMA Approved Dispositivos — 11 products
Publicidade
Total de dispositivos11
Categorias0
Última decisão da FDA
| Tipo | Número | Nome do dispositivo | Código | Data | Ações |
|---|---|---|---|---|---|
| 510(k) | K241128 | TDM Plate and Screw System | HRS | 2024-12-05 | Ver |
| 510(k) | K230071 | Femur Reconstruction Interlocking Nail System, Femur Retrograde Interlocking Nail System, Humerus Interlocking Nail System, Tibia Interlocking Nail System, Compression Hip Nail System | HSB | 2024-08-22 | Ver |
| 510(k) | K240423 | TDM Anterior Cervical Plate System | KWQ | 2024-04-08 | Ver |
| 510(k) | K232115 | TDM Large Bone Plate and Screw System | HRS | 2024-04-05 | Ver |
| 510(k) | K231860 | TDM Screw System | HWC | 2024-01-18 | Ver |
| 510(k) | K221844 | TDM Lumbar Interbody Fusion Cage System | MAX | 2022-08-17 | Ver |
| 510(k) | K220285 | PINE Pedicle Screw System | NKB | 2022-05-19 | Ver |
| 510(k) | K191057 | Park's Pectus System | HRS | 2020-03-19 | Ver |
| 510(k) | K190391 | TDM Plate and Screw Systems | HRS | 2019-11-15 | Ver |
| 510(k) | K190830 | TDM Screw Systems | HWC | 2019-09-13 | Ver |
| 510(k) | K171808 | TDM Plate and Screw System | HRS | 2018-03-15 | Ver |
Nenhum dispositivo correspondente.