While the Neurostep(TM) System is not currently available in the United States, Victhom is planning to engage with the U.S. Food and Drug Administration (FDA) to pursue plans for bringing this new solution for foot drop therapy to patients in the United States.
"Accomplishing CE Mark approval is the latest step in what continues to be the steady advance toward commercialization of the Neurostep(TM)", said Mr. Normand Rivard, Acting President of the Company. "These recent accomplishments are an indication of our commitment to this business and the ability of the Company to deliver on its scientific and business objectives", he added.
Victhom discovers, develops and manufactures bionic devices involved in the treatment of a variety of physical and physiological dysfunctions. Victhom's Neurobionix division focuses on the development and commercialization of technologies and products involving implantable devices that feature neurosensing and neurostimulation components, integrated with artificial intelligence. Victhom's Biotronix division develops biomechatronic products to support or replace peripheral limbs in what is known as the orthotics and prosthetics market.
Some of the statements made herein may constitute forward-looking statements. These statements relate to future events or our future financial performance and involve known and unknown risks, uncertainties and other factors that may cause Victhom's actual results, performance or achievements to be materially different from those expressed or implied by any of Victhom's statements. Actual events or results may differ materially. We disclaim any intention, and assume no obligation, to
|SOURCE VICTHOM HUMAN BIONICS INC.|
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