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 |