K242507
- 510(k) number
- K242507
- Device name
- OBSIDIO Conformable Embolic
- Applicant
- Boston Scientific MN · US
- Product code
- KRD — Device, Vascular, For Promoting Embolization
- Decision date
- 2024-10-03
- Date received
- 2024-08-22
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K242507.pdf
Official FDA record: K242507
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.