November 12, 2013

EndoShape's Medusa Vascular Plug Receives 510(k) Clearance

November 7, 2013—EndoShape (Boulder, CO) announced that it has received US Food and Drug Administration 510(k) marketing clearance for its Medusa vascular plug, a catheter-delivered device for arterial and venous embolization in the peripheral vasculature. The device occludes vessels in a single delivery sequence. The Medusa vascular plug is based on EndoShape's polymer material technology. The nonmetallic device produces minimal CT artifact. The Medusa vascular plug will be launched in the United States in early 2014, advised the company.

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November 12, 2013

EndoShape's Medusa Vascular Plug Receives 510(k) Clearance

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