Clariance has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market its Stand-Alone Anterior Lumbar Interbody Fusion Device: Idys®-ALIF ZP 3DTi. The design allows four fixation screws to be inserted through the cage and into the adjacent vertebral bodies to create a zero-profile stand-alone construct that removes the need for posterior fixation. Idys®-ALIF ZP 3DTi will be delivered in sterile packaging and available in multiple footprint, heights and lordotic angles.
