K251617
- 510(k) number
- K251617
- Device name
- X-PAC® TLIF Expandable Posterior Cage System; X-PAC® LLIF Expandable Lateral Cage System
- Applicant
- Expanding Innovations, Inc. CA · US
- Product code
- MAX — Intervertebral Fusion Device With Bone Graft, Lumbar
- Decision date
- 2025-06-16
- Date received
- 2025-05-27
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K251617.pdf
Official FDA record: K251617
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.