The following data is part of a premarket notification filed by Tdm Co. Ltd. with the FDA for Tdm Plate And Screw System.
Device ID | K171808 |
510k Number | K171808 |
Device Name: | TDM Plate And Screw System |
Classification | Plate, Fixation, Bone |
Applicant | TDM Co. Ltd. #F105-1.101-104, Sangsan-dong, 333 Cheonmdangwagi-ro, Buk-gu Gwangju, KR 61008 |
Contact | Babu Periasamy |
Correspondent | Babu Periasamy 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 | 2017-06-19 |
Decision Date | 2018-03-15 |
Summary: | summary |