K243609
- 510(k) number
- K243609
- Device name
- EquivaBone Osteoinductive Bone Graft Substitute (EquivaBone )
- Applicant
- Etex Corporation MA · US
- Product code
- MQV — Filler, Bone Void, Calcium Compound
- Decision date
- 2024-12-18
- Date received
- 2024-11-22
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K243609.pdf
Official FDA record: K243609
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.