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FDA approves Endologix Powerlink XL for large abdominal aortic aneurysms

This article was originally published in Clinica

Executive Summary

The US FDA has granted supplemental premarket approval (sPMA) for Endologix's Powerlink XL system for the treatment of abdominal aortic aneurysms (AAA) with larger neck diameters. The system is indicated for patients with aortic necks 23-32mm in diameter. Around 15% of AAA procedures are performed in patients with aortic necks measuring over 26mm, the Irvine, California firm says. The latest approval broadens the indications for the Powerlink endoluminal stent graft, which was originally approved in 2004 (see Clinica No 1091, p 16).

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