K242299
- 510(k) number
- K242299
- Device name
- NovaBone Putty - Synthetic Bioactive Bone Graft
- Applicant
- Novabone Products, LLC FL · US
- Product code
- MQV — Filler, Bone Void, Calcium Compound
- Decision date
- 2024-09-25
- Date received
- 2024-08-02
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K242299.pdf
Official FDA record: K242299
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.