Interventional technology firm Cook Medical has launched the Reform clinical trial, designed to evaluate its Formula balloon expandable stent for treating renal artery stenosis.
The trial will enroll up to 100 patients at up to 30 investigative sites throughout the U.S., according to the Bloomington, IN-based company. Initial results are expected to be available in the second quarter of 2010.
In other Cook news, the company has received U.S. Food and Drug Administration 510(k) clearance for its Celect vena cava filter. Celect is designed to prevent recurrent pulmonary embolism via placement in the vena cava, Cook said.
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