K243670
- 510(k) number
- K243670
- Device name
- Idys® LIF
- Applicant
- Clariance FR
- Product code
- MAX — Intervertebral Fusion Device With Bone Graft, Lumbar
- Decision date
- 2024-12-31
- Date received
- 2024-11-27
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.5 MB · U.S. public domain
Also available from FDA: K243670.pdf
Official FDA record: K243670
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.