BioStructures announces FDA approval for bone graft solution

BioStructures recently announced they have received FDA clearance for their new Silhouette MCS Bone Graft.

Indicated for better biologic responsiveness at the defect site and enhanced handling during the procedure, Silhouette is made of a bi-phasic mineral component within multiple type I collagen fibers. The company touts the graft allows for improved introduction of autogenic bone marrow aspirate, allowing for improved healing.

“We are very pleased to receive FDA clearance for Silhouette Mineralized Collagen Scaffold,” Russell Cook, chief executive officer of BioStructures, stated in a company release. “We founded BioStructures in 2009 with the goal to develop and commercialize proprietary first-in-class products in the bioactive, polymer, collagen and cellular bone graft spaces. The Silhouette clearance represents the third step in our attainment of that goal.”

“Looking forward, we will continue to develop our pipeline of products in a continued effort to offer a unique breadth of products all under the BioStructures umbrella.”

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