K240838
- 510(k) number
- K240838
- Device name
- Spectrum Spine Cervical Cage System
- Applicant
- Spectrum Spine, Inc. GA · US
- Product code
- ODP — Intervertebral Fusion Device With Bone Graft, Cervic
- Decision date
- 2024-05-30
- Date received
- 2024-03-27
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.1 MB · U.S. public domain
Also available from FDA: K240838.pdf
Official FDA record: K240838
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.