The FDA has approved the 510k clearance of Custom Spine’s Pathway AVID, which stands for articulating vertebral interbody device, according to a release from Custom Spine.
Pathway AVID consists of three intra-linked spacers, made from Peek-Optima, that are inserted into the disc space, then sequentially articulated to create an interbody that follows the natural curvature of the vertebra.
Read Custom Spine’s release on the FDA approval of Pathway AVID.
From findings on cervical disc replacement to total knee replacement, Becker’s reported on eight spine and orthopedic studies since March…
Researchers at UMass Chan Medical School in Worcester, Mass., have created an algorithm to predict total knee replacement outcomes in…
Orthopaedic Solutions Management has acquired Orlando Hand Surgical Associates, marking its eighth acquisition. OHSA was founded in 2000 and has…
Comments are closed.