K242557
- 510(k) number
- K242557
- Device name
- ClotTriever XL Catheter (41-102)
- Applicant
- Inari Medical, Inc. CA · US
- Product code
- QEW — Peripheral Mechanical Thrombectomy With Aspiration
- Decision date
- 2024-09-27
- Date received
- 2024-08-28
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K242557.pdf
Official FDA record: K242557
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.