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Aptus Endosystems Receives Heli-FX FDA Approval

Wednesday, May 29, 2013 5:17:00 AM PDT | VentureDeal

   Sunnyvale, California  --  Medical device maker Aptus Endosystems said that it has received 510(k) marketing clearance from the US FDA for its Heli-FX Guide.

Designed as a line extension of the company's original Heli-FX System, the guide is a 28 mm tip that enhances treatment of wide neck abdominal aortic aneurysms (AAA).

The longer reach tip gives physicians greater ability to implant anchors improve the long-term durability of difficult to treat aortic anatomy.

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