K262595
- 510(k) number
- K262595
- Device name
- VariLift-C Cervical Interbody Fusion System
- Applicant
- Wenzel Spine, Inc. TX · US
- Product code
- ODP — Intervertebral Fusion Device With Bone Graft, Cervic
- Decision date
- 2026-08-26
- Date received
- 2026-07-27
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.1 MB · U.S. public domain
Also available from FDA: K262595.pdf
Official FDA record: K262595
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.