Nexxt Spine Gains FDA Clearance for ALIF and Lateral Systems

By Julie A. Vetalice

Nexxt Spine Gains FDA Clearance for ALIF and Lateral Systems

Nexxt Spine was granted FDA 510(k) clearance to market ALIF and Lateral lumbar systems. Alpha launch is slated for 3Q20, with integrated plate systems coming in 4Q20.

Both systems feature Nexxt Matrixx® 3D-printed titanium technology to create the desired pore size and geometry, and have a modulus of elasticity lower than PEEK, a microroughened surface and a 75% porous lattice.

“We are thrilled to be releasing these two powerhouses this year,” said President Andy Elsbury. “Our engineering and 3D printing manufacturing teams has been working diligently to simultaneously develop and clear the two products after considerable surgeon demand for Nexxt Spine quality clinical outcomes for ALIF and Lateral approaches.”

Product Labels: Lumbar Spine, Spinal Fusion

Tags: 510(k) Clearance, Regulatory