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SpineEX Gains FDA Clearance for Sagittae LLIF -

SpineEX received FDA 510(k) clearance to market its Sagittae® expandable device for minimally invasive lateral lumbar interbody fusion. Sagittae is available in five sizes designed for up to 8mm of continuous in situ expansion, with up to 30° of continuous in situ lordotic adjustment. A large single chamber can be filled with bone graft after insertion and adjustment to ensure even contact with both vertebral endplates. (SpineEX, Inc., 10/10/18)