FDA 510(k) Applications Submitted by TDM Co., Ltd.

FDA 510(k) Number Submission Date Device Name Applicant
K240423 02/13/2024 TDM Anterior Cervical Plate System TDM Co., Ltd.
K230071 01/10/2023 Femur Reconstruction Interlocking Nail System, Femur Retrograde Interlocking Nail System, Humerus Interlocking Nail System, Tibia Interlocking Nail System, Compression Hip Nail System TDM CO., LTD.
K231860 06/23/2023 TDM Screw System TDM Co., Ltd.
K241128 04/24/2024 TDM Plate and Screw System TDM Co., Ltd.


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