Cordis scores U.S., EU regulatory wins for balloon catheter

06/27/2013 | MassDevice.com (Boston)

Cordis, a unit of Johnson & Johnson, has received 510(k) clearance in the U.S. and CE mark approval in Europe for the new 20-millimeter and 280-millimeter sizes of its Sleek OTW balloon catheter. The device, designed to clear blockages in below-the-knee arteries, is intended to help patients avoid lower-limb amputations.

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