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Aptus Endosystems lands FDA nod for abdominal aneurysm device

Thu, 09/20/2012 - 2:53pm
Mass Device

Aptus Endosystems lands 510(k) clearance from the FDA for its thoracic-length HeliFX aortic anchor for repairing abdominal aortic aneurysms.

Aptus Endosystems lands FDA nod for abdominal aneurysm device
Aptus Endosystems said it won 510(k) clearance from the FDA for its thoracic-length HeliFX aortic anchor for repairing abdominal aortic aneurysms. The first iteration of the device earned FDA clearanceand its share of controversy – in November 2011. The latest clearance came via the watchdog agency's de novo device review protocol. Aptus counts former Boston Scientific (NYSE:BSX) CEO James Tobin as a member of its board of directors.

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