K242826
- 510(k) number
- K242826
- Device name
- ProLift Wedge Expandable Spacer System
- Applicant
- Life Spine, Inc. IL · US
- Product code
- MAX — Intervertebral Fusion Device With Bone Graft, Lumbar
- Decision date
- 2024-10-08
- Date received
- 2024-09-18
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.9 MB · U.S. public domain
Also available from FDA: K242826.pdf
Official FDA record: K242826
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.