SpineVision Receives FDA Clearance, CE Mark for Interbody Cage

September 18, 2018

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.

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