Baxter Announces FDA Approval Of ARTISS Slow Setting Fibrin

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Baxter Announces FDA Approval Of ARTISS Slow Setting Fibrin

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03-22-2008, 01:00 PM

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Baxter Announces FDA Approval Of ARTISS Slow Setting Fibrin

Baxter Healthcare Corporation announced the U.S. Food and Drug Administration (FDA) approval of ARTISS (Fibrin Sealant (Human)), the first and only slow-setting fibrin sealant indicated for use in adhering skin grafts in adult and pediatric burn patients. ARTISS was developed using Baxter's proven fibrin sealant technology platform and is the newest agent in the company's expanding BioSurgery portfolio.
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