Tdm Co., Ltd.
FDA 510(k) & PMA Approved Devices — 11 products
Total Devices11
Categories6
Latest Approval2024-12-05
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K241128 | TDM Plate and Screw System | HRS | 2024-12-05 | View |
| 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 | View |
| 510(k) | K240423 | TDM Anterior Cervical Plate System | KWQ | 2024-04-08 | View |
| 510(k) | K232115 | TDM Large Bone Plate and Screw System | HRS | 2024-04-05 | View |
| 510(k) | K231860 | TDM Screw System | HWC | 2024-01-18 | View |
| 510(k) | K221844 | TDM Lumbar Interbody Fusion Cage System | MAX | 2022-08-17 | View |
| 510(k) | K220285 | PINE Pedicle Screw System | NKB | 2022-05-19 | View |
| 510(k) | K191057 | Park's Pectus System | HRS | 2020-03-19 | View |
| 510(k) | K190391 | TDM Plate and Screw Systems | HRS | 2019-11-15 | View |
| 510(k) | K190830 | TDM Screw Systems | HWC | 2019-09-13 | View |
| 510(k) | K171808 | TDM Plate and Screw System | HRS | 2018-03-15 | View |
No matching devices.