K240507
- 510(k) number
- K240507
- Device name
- NuVasive AttraX Scaffold
- Applicant
- Nuvasive, Inc. CA · US
- Product code
- MQV — Filler, Bone Void, Calcium Compound
- Decision date
- 2024-03-20
- Date received
- 2024-02-21
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K240507.pdf
Official FDA record: K240507
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.