Excipio SV Thrombectomy Device— 510(k) K221204

Substantially Equivalent

Contego Medical, Inc.

FDA 510(k) clearance K221204 for Excipio SV Thrombectomy Device, Substantially Equivalent on 2022-06-23. Applicant: Contego Medical, Inc..

Clearance details

Applicant: Contego Medical, Inc.
Product code: Code QEW
Advisory panel: Cardiovascular
Date received: 2022-04-26
Decision date: 2022-06-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Raleigh, NC, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code QEW

product code QEW

Death: 126
Injury: 282
Malfunction: 820
Total: 1,228

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.