K250421
- 510(k) number
- K250421
- Device name
- InThrill Thrombectomy System
- Applicant
- Inari Medical, Inc. CA · US
- Product code
- QEW — Peripheral Mechanical Thrombectomy With Aspiration
- Decision date
- 2025-05-12
- Date received
- 2025-02-13
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 3.0 MB · U.S. public domain
Also available from FDA: K250421.pdf
Official FDA record: K250421
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.