Spineart received CE Mark Approval for its JULIET®Ti lumbar interbody systems featuring TI-LIFE, a micro-porous scaffold designed to mimic trabecular bone.
Produced via additive manufacturing, TI-LIFE features interconnected pores of 600 μm to 700 μm with an overall porosity of 70% to 75%, and is designed to enable cell colonization and promote bone in-growth.
Like all Spineart implants, the JULIET Ti range is sterile-packed and barcoded for safety, procedure compliance and cost-efficiency.
Other 3D-printed/additively-manufactured interbody devices in the news since 4Q15 include:
4WEB Medical’s Posterior Spine Truss
K2M’s Lamellar Titanium Technology
Renovis Surgical’s Tesera SC Cervical Interbody Fusion System
Stryker Spine’s Tritanium Posterior Lumbar Cage
Spineart received CE Mark Approval for its JULIET®Ti lumbar interbody systems featuring TI-LIFE, a micro-porous scaffold designed to mimic trabecular bone.
Produced via additive manufacturing, TI-LIFE features interconnected pores of 600 μm to 700 μm with an overall porosity of 70% to 75%, and is designed to enable cell colonization and...
Spineart received CE Mark Approval for its JULIET®Ti lumbar interbody systems featuring TI-LIFE, a micro-porous scaffold designed to mimic trabecular bone.
Produced via additive manufacturing, TI-LIFE features interconnected pores of 600 μm to 700 μm with an overall porosity of 70% to 75%, and is designed to enable cell colonization and promote bone in-growth.
Like all Spineart implants, the JULIET Ti range is sterile-packed and barcoded for safety, procedure compliance and cost-efficiency.
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