K240765
- 510(k) number
- K240765
- Device name
- Porous Biologic Scaffold
- Applicant
- Ventris Medical CA · US
- Product code
- MQV — Filler, Bone Void, Calcium Compound
- Decision date
- 2024-12-18
- Date received
- 2024-03-20
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.6 MB · U.S. public domain
Also available from FDA: K240765.pdf
Official FDA record: K240765
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.