K242509
- 510(k) number
- K242509
- Device name
- HAnano InterFuse(R) Modular Interbody
- Applicant
- Next Orthosurgical CA · US
- Product code
- MAX — Intervertebral Fusion Device With Bone Graft, Lumbar
- Decision date
- 2024-09-19
- Date received
- 2024-08-22
- 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: K242509.pdf
Official FDA record: K242509
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.