FLIXENE IFG VASCULAR GRAFT— 510(k) K130142

Substantially Equivalent

Atrium Medical Corporation

FDA 510(k) clearance K130142 for FLIXENE IFG VASCULAR GRAFT, Substantially Equivalent on 2013-03-15. Applicant: Atrium Medical Corporation.

Clearance details

Applicant: Atrium Medical Corporation
Product code: Code DSY
Advisory panel: Cardiovascular
Date received: 2013-01-22
Decision date: 2013-03-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hudson, NH, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code DSY

product code DSY

Death: 29
Injury: 694
Total: 723

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.