December 14, 2010
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Aesculap begins market evaluation of new advanced knee replacement technology

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Aesculap announced in a press release that its VEGA System, an advanced knee replacement technology system, was recently cleared for marketing by the FDA. The VEGA System offers advanced knee replacement technologies, including multilayer coating and a unique kinematic design, the company reported.

The market evaluation phase commenced in November 2010 with the first surgery. Early clinical results are positive with further evaluation ongoing, Aesculap said. The market evaluation is estimated to conclude in the 1st Quarter of 2011 with anticipated market availability in the 3rd quarter 2011. The company is also preparing to begin evaluations in Europe and Asia later this year, according to the press release.