Nexxt Spine gains clearance for 2 lumbar systems; plans Q3 launch

The FDA on May 28 issued 510(k) clearance for Nexxt Spine’s anterior lumbar interbody fusion and lateral implants.

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Four things to know:

1. Nexxt Spine plans to resume in-house manufacturing of the two systems.

2. The ALIF and lateral systems feature the company’s Nexxt Matrixx 3D-printed titanium technology. 

3. They are designed with a modulus of elasticity lower than PEEK and a 75 percent porous lattice.

4. Nexxt Spine will launch both products in the third quarter.

More articles on devices:
How 5 spine practices are proceeding with recovery plans
New Jersey hospital opens Institute for Robotic Surgery
Centinel Spine gets OK for manufacturing transfer of prodisc systems

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