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See Latest ArticlesCryoLife Receives FDA Approval to Begin U.S. Clinical Trial for BioFoam
Cryolife, 10/28/09
CryoLife, Inc., an implantable biological medical device and cardiovascular tissue processing company, announced that the U.S. Food and Drug Administration has granted approval for the company's Investigational Device Exemption to conduct a human clinical trial for its BioFoam Surgical Matrix protein hydrogel technology. BioFoam will be used to help seal liver parenchymal tissue when cessation of bleeding by ligature or other conventional methods is ineffective or impractical.
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