K251207
- 510(k) number
- K251207
- Device name
- Sangria Thrombectomy System
- Applicant
- Avantec Vascular Corporation CA · US
- Product code
- QEW — Peripheral Mechanical Thrombectomy With Aspiration
- Decision date
- 2026-01-07
- Date received
- 2025-04-18
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K251207.pdf
Official FDA record: K251207
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.