K261067
- 510(k) number
- K261067
- Device name
- BEE PLIF Cage
- Applicant
- NGMedical GmbH DE
- Product code
- MAX — Intervertebral Fusion Device With Bone Graft, Lumbar
- Decision date
- 2026-04-30
- Date received
- 2026-04-01
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.2 MB · U.S. public domain
Also available from FDA: K261067.pdf
Official FDA record: K261067
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.