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 ...
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Discover the latest FDA-cleared orthopedic and spine devices and technologies, including robotics, implants, and bone graft systems.
Backpack® AMP is supplied in a ported pouch for easy hydration and is ready to use, simplifying the surgical process. John Brunelle, PhD, COO of Ventris Medical added: "The Backpack® technology ...
Ventris Medical, a privately held orthobiologics and tissue regeneration company, today announced that the United States Food and Drug Administration has granted 510(k) clearance for Backpack® (Porous ...
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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 ...