www.fdanews.com/articles/183886-nexxt-spine-announces-fda-clearance-for-the-nexxt-matrixx-system
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Nexxt Spine Announces FDA Clearance for the Nexxt Matrixx System
October 9, 2017
Nexxt Spine received 510(k) marketing clearance for its Nexxt Matrixx System. The 3D printed porous titanium system creates interbody and vertebral body replacement devices that allow for radiographic imaging.
Nexxt Spine combined its proprietary, residue-free, surface technology with open porosity, providing more surface area for bone apposition than conventional spinal implants.
The 3D printed products can accommodate the anatomic and clinical circumstances of each patient.