K233947
- 510(k) number
- K233947
- Device name
- KLIMT Expandable Lumbar Interbody Fusion (LIF) Cage System
- Applicant
- Ctl Medical Corporation TX · US
- Product code
- MAX — Intervertebral Fusion Device With Bone Graft, Lumbar
- Decision date
- 2024-10-10
- Date received
- 2023-12-14
- 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: K233947.pdf
Official FDA record: K233947
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.