Orthovita Announces FDA 510k Clearance to Market VITOSS Scaffold FOAM Bone Graft Material.
Business Wire (January 12, 2004)
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Orthovita Announces FDA 510k Clearance to Market VITOSS Scaffold FOAM Bone Graft Material.
Business Editors/Health/Medical Writers
MALVERN, Pa.--(BUSINESS WIRE)--Jan. 12, 2004 Clearance of New Biomaterial Platform Co-developed with Kensey Nash Corporation Expected to Enable Commercialization of a Wide Array of New Products to Treat Bone Defects Caused by Injury or Trauma Orthovita, Inc. (NASDAQ NM:VITA), a leading developer of orthopaedic biomaterials, reported today it has received 510(k) F...Try vLex for FREE for 3 days
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