Determination of Regulatory Review Period for Purposes of Patent Extension; PRO OSTEONSUPTM Implant 500 Coralline Hydroxyapatite Bone Void Filler

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The Food and Drug Administration (FDA) has determined the regulatory review period for PRO OSTEON TM Implant 500 Coralline Hydroxyapatite Bone Void Filler and is publishing this notice of that determination as required by law. FDA has made the determination because of the submission of an application to the Commissioner of Patents and Trademarks, Department of Commerce, for the extension of a patent which claims that medical device.