K240404
- 510(k) number
- K240404
- Device name
- NovaBone Putty - Bioactive Synthetic Bone Graft (NB6600, NB6610, NB6615)
- Applicant
- Novabone Products, LLC FL · US
- Product code
- MQV — Filler, Bone Void, Calcium Compound
- Decision date
- 2024-03-05
- Date received
- 2024-02-09
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.3 MB · U.S. public domain
Also available from FDA: K240404.pdf
Official FDA record: K240404
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.