ANGIOJET SOLENT PROXI THROMBECTOMY SET MODEL 109676-001— 510(k) K101406

Substantially Equivalent

Medrad Interventional/Possis

FDA 510(k) clearance K101406 for ANGIOJET SOLENT PROXI THROMBECTOMY SET MODEL 109676-001, Substantially Equivalent on 2010-06-16. Applicant: Medrad Interventional/Possis.

Clearance details

Applicant: Medrad Interventional/Possis
Product code: Code QEZ
Advisory panel: Cardiovascular
Date received: 2010-05-19
Decision date: 2010-06-16
Decision: Substantially Equivalent
Clearance type: Special
Location: Minneapolis, MN, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code QEZ

product code QEZ

Death: 24
Total: 24

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.