Item 8.01 Other Events

On June 8, 2009, the U.S. Food and Drug Administration granted 510(k) clearance for Orthovita, Inc.'s CORTOSS™ Bone Augmentation Material in the treatment of vertebral compression fractures. The press release announcing the clearance is being furnished with this Current Report on Form 8-K as Exhibit 99.1 and is hereby incorporated herein by reference.

Item 9.01 Financial Statements and Exhibits

(d) Exhibits

Exhibit No. Description
99.1 Press Release, dated June 8, 2009, issued by Orthovita, Inc.

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