Spineart is pleased to announce that it has received 510(k) clearance from the FDA to market its new JULIET®Ti lumbar interbody systems in the United States. The JULIET®Ti PO, OL and TL interbody systems are the first range of titanium interbody implants benefiting from our proprietary Ti-LIFETechnology1.  Ti-LIFETechnology micro-porous scaffold mimics the bone trabecular structure and features interconnected pores of 600 μm to […]