Nexxt Spine Gains FDA Clearance for NEXXT MATRIXX Devices

By Julie A. Vetalice

Nexxt Spine received FDA 510(k) clearance to market 3D-printed NEXXT MATRIXX™ interbody and vertebral body replacement devices.

The implants are based on Nexxt Spine's proprietary residue-free surface technology with varied porosity titanium architecture. Compared to conventional spine devices, the company clains that NEXXT MATRIXX implants exhibit up to 4x more surface area for bone formation and up to 2x more open pore volume. Additional NEXXT MATRIXX-based systems will be launched this and next year.

Source: Nexxt Spine, LLC

Image courtesy of Nexxt Spine

Product Labels: Spinal Fusion

Tags: 510(k) Clearance, Regulatory