MSN による配信15 日
FDA grants 510(k) clearance to Ventris Medical’s Backpack for orthopaedic use
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 ...
Morningstar17 日
Ventris Medical Receives 510(k) Clearance for Innovative Backpack® Bone Graft Containment ...
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 ...