K250787
- 510(k) number
- K250787
- Device name
- Liberant Thrombectomy System
- Applicant
- Medtronic, Ireland IE
- Product code
- QEW — Peripheral Mechanical Thrombectomy With Aspiration
- Decision date
- 2025-06-11
- Date received
- 2025-03-14
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K250787.pdf
Official FDA record: K250787
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.