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Nanovis Gains FDA Clearance of FortiCore Interbodies with Nanosurface Technology -

Nanovis received FDA 510(k) clearance to market FortiCore® interbody fusion devices that feature a Nanosurface-enhanced porous titanium scaffold, intermolded with a PEEK core. The devices are intended for use in transforaminal and anterior lumbar interbody fusion procedures (TLIF and ALIF). The nanopatterned surface is intended to target fixation-related complications; it also forms the basis of a bactericidal program under development to address infection-related complications. (Nanovis, 3/28/18)