K233366
- 510(k) number
- K233366
- Device name
- SYMPHONY OCT System
- Applicant
- Medos International SARL CH
- Product code
- NKG — Posterior Cervical Screw System
- Decision date
- 2023-11-09
- Date received
- 2023-10-02
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
510(k) Summary (official FDA PDF): K233366.pdf
Official FDA record: K233366
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.