Spineart receives clearance from the fda to market its ti-life technology 3d titanium interbody devices

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 700 μm and an overall porosity of 70-75% designed to enable cell colonization and promote bone in-growth2.

This technology is based on a unique algorithm associated with a state-of-the-art additive manufacturing process, often referred to as 3D printing.

The JULIET®Ti PO, OL and TL interbody systems include a full range of sizes to address different anatomies. The smooth bullet-shaped nose, lateral sides and chamfers of the implant are polished to preserve endplates, nerve roots and soft tissues during insertion.

The JULIET®Ti design features an overall reduced density to optimize imaging performance.

In accordance with the Spineart philosophy, the instrument set is ultra-compact and features multi-functional instruments.

All Spineart implants, including the entire JULIET®Ti range, are sterile packed and barcoded for increased safety, procedure compliance and cost-efficiency.

For distribution opportunities please contact us at contact@spineart.com or visit spineart.com/distributorsUSA.

1Filed patent

2Pre-clinical data may not represent clinical results.

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