K243814
- 510(k) number
- K243814
- Device name
- NuVasive Pulse System
- Applicant
- Globus Medical, Inc. PA · US
- Product code
- OLO — Orthopedic Stereotaxic Instrument
- Decision date
- 2025-01-10
- Date received
- 2024-12-11
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 3.1 MB · U.S. public domain
Also available from FDA: K243814.pdf
Official FDA record: K243814
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.