K252240
- 510(k) number
- K252240
- Device name
- Spectrum Spine Cervical Cage System; Spectrum Spine Lumbar Cage System
- Applicant
- Spectrum Spine GA · US
- Product code
- ODP — Intervertebral Fusion Device With Bone Graft, Cervic
- Decision date
- 2026-03-30
- Date received
- 2025-07-17
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K252240.pdf
Official FDA record: K252240
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.