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SpineVision Gains FDA Clearance, CE Mark for HEXANIUM TLIF Cage -

SpineVision received FDA 510(k) clearance and CE Mark approval for its 3D-printed, titanium HEXANIUM transforaminal lumbar interbody fusion (TLIF) cage. The next generation HEXANIUM TLIF cage combines a titanium surface—designed for rapid osseointegration—along with a porous, honeycomb-like structure to maximize bone ingrowth and ongrowth from endplate to endplate, according to SpineVision. The cage is also designed to reduce the risk of subsidence in disc height, post-op. (SpineVision, 9/17/18)