K231860
- 510(k) number
- K231860
- Device name
- TDM Screw System
- Applicant
- Tdm Co., Ltd. KR
- Product code
- HWC — Screw, Fixation, Bone
- Decision date
- 2024-01-18
- Date received
- 2023-06-23
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 3.2 MB · U.S. public domain
Also available from FDA: K231860.pdf
Official FDA record: K231860
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.