K240261
- 510(k) number
- K240261
- Device name
- Siege Vascular Plug (SVP2.5-0.021); Siege Vascular Plug (SVP4-0.021); Siege Vascular Plug (SVP6-0.027)
- Applicant
- Merit Medical Systems, Inc. UT · US
- Product code
- KRD — Device, Vascular, For Promoting Embolization
- Decision date
- 2024-05-02
- Date received
- 2024-01-31
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K240261.pdf
Official FDA record: K240261
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.