NuVasive Wins Expanded 510(k) Clearance for TLX Interbody System

October 18, 2017

NuVasive received an expanded FDA 510(k) clearance for its TLX interbody system for  spinal fusion surgery.

The new clearance introduces an expandable 20 degree cage and broader indications for use, including use with allogeneic bone graft and in additional levels of the spine.

The system is inserted using a conventional lumbar interbody fusion.

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