K240423
- 510(k) number
- K240423
- Device name
- TDM Anterior Cervical Plate System
- Applicant
- Tdm Co., Ltd. KR
- Product code
- KWQ — Appliance, Fixation, Spinal Intervertebral Body
- Decision date
- 2024-04-08
- Date received
- 2024-02-13
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K240423.pdf
Official FDA record: K240423
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.