K250446
- 510(k) number
- K250446
- Device name
- Frida Anterior Cervical Plate System
- Applicant
- Spineup, Inc. FL · US
- Product code
- KWQ — Appliance, Fixation, Spinal Intervertebral Body
- Decision date
- 2025-05-23
- Date received
- 2025-02-14
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K250446.pdf
Official FDA record: K250446
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.