K250560
- 510(k) number
- K250560
- Device name
- BEE HA
- Applicant
- NGMedical GmbH DE
- Product code
- ODP — Intervertebral Fusion Device With Bone Graft, Cervic
- Decision date
- 2025-11-21
- Date received
- 2025-02-25
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 3.1 MB · U.S. public domain
Also available from FDA: K250560.pdf
Official FDA record: K250560
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.