K260479
- 510(k) number
- K260479
- Device name
- TheraSphere 360 Y-90 Management Platform
- Applicant
- Boston Scientific Corporation MA · US
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2026-03-13
- Date received
- 2026-02-13
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K260479.pdf
Official FDA record: K260479
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.