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 |