Tdm Co., Ltd.
FDA 510(k) & PMA Approved Produkte — 11 products
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Produkte insgesamt11
Kategorien0
Neueste FDA-Entscheidung
| Typ | Nummer | Produktname | Code | Datum | Aktionen |
|---|---|---|---|---|---|
| 510(k) | K241128 | TDM Plate and Screw System | HRS | 2024-12-05 | Anzeigen |
| 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 | Anzeigen |
| 510(k) | K240423 | TDM Anterior Cervical Plate System | KWQ | 2024-04-08 | Anzeigen |
| 510(k) | K232115 | TDM Large Bone Plate and Screw System | HRS | 2024-04-05 | Anzeigen |
| 510(k) | K231860 | TDM Screw System | HWC | 2024-01-18 | Anzeigen |
| 510(k) | K221844 | TDM Lumbar Interbody Fusion Cage System | MAX | 2022-08-17 | Anzeigen |
| 510(k) | K220285 | PINE Pedicle Screw System | NKB | 2022-05-19 | Anzeigen |
| 510(k) | K191057 | Park's Pectus System | HRS | 2020-03-19 | Anzeigen |
| 510(k) | K190391 | TDM Plate and Screw Systems | HRS | 2019-11-15 | Anzeigen |
| 510(k) | K190830 | TDM Screw Systems | HWC | 2019-09-13 | Anzeigen |
| 510(k) | K171808 | TDM Plate and Screw System | HRS | 2018-03-15 | Anzeigen |
Keine passenden Geräte.