K254130
- 510(k) number
- K254130
- Device name
- C.A. Medical Interbody Fusion System
- Applicant
- C.A. Medical, LLC TX · US
- Product code
- ODP — Intervertebral Fusion Device With Bone Graft, Cervic
- Decision date
- 2026-07-08
- Date received
- 2025-12-22
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K254130.pdf
Official FDA record: K254130
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.