Life Spine received FDA 510(k) clearance to market the PROLIFT® Expandable Interbody System for use in minimally invasive PLIF, TLIF and oblique approaches.
PROLIFT is scheduled for limited release in 2Q16, with full product release expected later in 2016.
Life Spine received FDA 510(k) clearance to market the PROLIFT® Expandable Interbody System for use in minimally invasive PLIF, TLIF and oblique approaches.
PROLIFT is scheduled for limited release in 2Q16, with full product release expected later in 2016.
Life Spine received FDA 510(k) clearance to market the PROLIFT® Expandable Interbody System for use in minimally invasive PLIF, TLIF and oblique approaches.
PROLIFT is scheduled for limited release in 2Q16, with full product release expected later in 2016.
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