SpineVision Receives FDA Clearance, CE Mark for Interbody Cage

French devicemaker SpineVision was granted 510(k) clearance from the FDA and the CE Mark for its titanium 3D laser-printed Hexanium interbody fusion cage for use in back surgery.

The transforaminal lumbar interbody fusion (TLIF) cage is used to fuse two vertebrae together and stop the movement of a painful segment in the spine.

The cage’s titanium surface promotes connection between bone and cage, and its honeycomb structure has large windows for maximum bone in-growth and on-growth between the cage’s endplates.