The following data is part of a premarket notification filed by Tdm Co. Ltd. with the FDA for Tdm Plate And Screw Systems.
Device ID | K190391 |
510k Number | K190391 |
Device Name: | TDM Plate And Screw Systems |
Classification | Plate, Fixation, Bone |
Applicant | TDM Co. Ltd. 69, Cheomdan Venture So-ro, 37 Beon-gil, Buk-gu Gwangju, KR 61003 |
Contact | Yougdae Kim |
Correspondent | Sevrina Ciucci Lince Consulting LLC 111 Deerwood Road, Suite 200 San Ramon, CA 94583 |
Product Code | HRS |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2019-02-19 |
Decision Date | 2019-11-15 |