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

FDA 510(k) Number Submission Date Device Name Applicant
K171808 06/19/2017 TDM Plate and Screw System TDM Co. Ltd.
K220285 02/01/2022 PINE Pedicle Screw System TDM Co. Ltd.
K191057 04/22/2019 Park's Pectus System TDM Co. Ltd.
K190391 02/19/2019 TDM Plate and Screw Systems TDM Co. Ltd.
K190830 04/01/2019 TDM Screw Systems TDM Co. Ltd.


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