Axis Spine Technologies (AST) today announces it has received FDA 510(k) clearance for standalone use + extended applications of its differentiating modular ALIF device.
AST is the first company to now offer up to 40 degrees lordotic cages, as well as up to 20 degrees of coronally tapered endplates, allowing surgeons a range of correction capabilities far in excess of any other interbody implant, when treating lumbar degenerative and deformity patients.
Axis-ALIF is currently available for sale in the United States.
