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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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