The US Food and Drug Administration (FDA) has granted 510(k) clearance to Ventris Medical’s Backpack (Porous Biologic Scaffold, K240765) for orthopaedic and spinal fusion procedures. Designed to ...
Russell Cook, CEO of Ventris Medical commented, "We are very pleased to receive FDA clearance for both the Backpack® AF and Backpack® AMP Bone Graft Systems. This graft containment technology is ...
Backpack ® AMP is supplied in a ported pouch for easy hydration and is ready to use, simplifying the surgical process.
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