The following data is part of a premarket notification filed by Tdm Co. Ltd. with the FDA for Tdm Screw Systems.
| Device ID | K190830 | 
| 510k Number | K190830 | 
| Device Name: | TDM Screw Systems | 
| Classification | Screw, Fixation, Bone | 
| Applicant | TDM Co. Ltd. 69, Cheomdan Venture So-ro, 37 Beon-gil, Buk-gu Gwangju, KR 61003 | 
| Contact | Youngdae Kim | 
| Correspondent | Sevrina Ciucci Lince Consulting LLC 111 Deerwood Road, Suite 200 San Ramon, CA 94583  | 
| Product Code | HWC | 
| CFR Regulation Number | 888.3040 [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Traditional | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 2019-04-01 | 
| Decision Date | 2019-09-13 | 
| Summary: | summary |