K240749
- 510(k) number
- K240749
- Device name
- PILLAR SA Ti Spacer System (82-XXX)
- Applicant
- Orthofix, Inc. TX · US
- Product code
- MAX — Intervertebral Fusion Device With Bone Graft, Lumbar
- Decision date
- 2024-05-28
- Date received
- 2024-03-19
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 2.0 MB · U.S. public domain
Also available from FDA: K240749.pdf
Official FDA record: K240749
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.