BioStructures Receives FDA 510(k) Clearance for Signafuse Bioactive Bone Graft Putty

 
BioStructures announced the U.S. Food and Drug Administration has granted 510(k) clearance for Signafuse Bioactive Bone Graft Putty. 

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Signafuse is indicated for the posterolateral spine, extremities and pelvis as well as a bone graft extender in the posterolateral spine. It is comprised of a biphasic mineral and bioactive glass suspended in a resorbable polymer carrier.

 

BioStructures is a privately held orthobiologics company.

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