K240889
- 510(k) number
- K240889
- Device name
- ARTFX Lumbar PEEK Cages
- Applicant
- Artfx Medical FL · US
- Product code
- MAX — Intervertebral Fusion Device With Bone Graft, Lumbar
- Decision date
- 2024-10-02
- Date received
- 2024-04-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K240889.pdf
Official FDA record: K240889
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.