Clearance as a bone void filler for use in the posterolateral spine
Third FDA clearance for MagnetOs in the last 7 months
Product provides opportunity to de-risk U.S. commercialization plans
Kuros Biosciences (“Kuros” or the “Company”), a leader in next generation bone graft technologies, announced today that its MagnetOs Flex Matrix has been cleared by the U.S. Food and Drug Administration (FDA) as a bone void filler for use in the posterolateral spine.
MagnetOs Flex Matrix is a new open matrix bone graft with a unique fibrillar and flexible structure that optimizes the effect of Kuros' established pro-healing NeedleGripTM surface technology
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