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 |