K232611
- 510(k) number
- K232611
- Device name
- TruLift Micro Expandable Spacer System & TruLift Expandable Spacer System
- Applicant
- Life Spine, Inc. IL · US
- Product code
- MAX — Intervertebral Fusion Device With Bone Graft, Lumbar
- Decision date
- 2023-11-30
- Date received
- 2023-08-28
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K232611.pdf
Official FDA record: K232611
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.