K234008
- 510(k) number
- K234008
- Device name
- CERAMENT G
- Applicant
- Bonesupport AB SE
- Product code
- QRR — Filler, Bone Void, Calcium Compound Containing Singl
- Decision date
- 2024-03-13
- Date received
- 2023-12-19
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K234008.pdf
Official FDA record: K234008
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.