Orthovita Submits 510(k) Application To FDA For The Use Of CORTOSS(R) Bone Augmentation Material In Vertebral Augmentation

Orthovita, Inc. (NASDAQ:VITA), a spine and orthopedic biosurgery company, announced that it has submitted a 510(k) filing to the U.S. Food and Drug Administration for the use of its CORTOSS Bone Augmentation Material in vertebral augmentation. This filing is based on data collected in three U.S.

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Filed under: Bones on January 17th, 2008