K233360
- 510(k) number
- K233360
- Device name
- Curiteva Thoracolumbar Plate System
- Applicant
- Curiteva, Inc. AL · US
- Product code
- KWQ — Appliance, Fixation, Spinal Intervertebral Body
- Decision date
- 2024-02-29
- Date received
- 2023-09-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
510(k) Summary (official FDA PDF): K233360.pdf
Official FDA record: K233360
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.