Aurora Spine Corporation announced that a Peer-Reviewed Clinical Publication titled ‘Improving the Management of Patients with Osteoporosis Undergoing Spinal Fusion: The Need for a Bone Mineral Density-Matched Interbody Cage, was published in Orthopedic Research and Reviews. The research article provides an introductory profile of a spinal interbody implant designed to simulate the lattice structure of human cancellous bone, with a similar modulus of elasticity, and specialized to match a patient’s bone status across the bone mineral density (BMD) continuum. The implant incorporates an open pore design where the degree of pore compactness directly corresponds to the patient’s dual x-ray absorptiometry (DXA)-defined BMD status, including patients with osteoporosis. An implant that fits this criterion is Aurora’s DEXA TiBone™ (also known as DEXA-C), a spinal interbody implant that received 510(k) premarket notification for commercial use in the US in August 2021.