Clariance has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market the Anterior Lumbar Interbody Fusion Device: Idys®-ALIF 3DTi. This cage connects to a cleverly designed plate that allows surgeons to insert screws within a wide range of angulation ensuring strong anchorage of the system.
Idys®-ALIF 3DTi will be delivered in sterile packaging and available in multiple footprint, heights and lordotic angles.