Centinel Spine Gains FDA Clearance of FLX 3D Printed Titanium Interbodies

By Julie A. Vetalice

Centinel Spine received FDA 510(k) clearance to market the FLX™ platform of Integrated Interbody™ and non-integrated 3D-printed, all-titanium interbody fusion devices.

FLX is based on the company's established STALIF interbody devices, in a novel all-titanium lattice option. FLX devices feature solid and porous radiolucent sections designed to offer less mechanical stiffness and better visibility vs. solid titanium implants, as well as a proprietary FUSE-THRU™ trabecular scaffold for bony in-growth and on-growth.

Source: Centinel Spine, LLC

Centinel Spine 3D Printed Technology

Image courtesy of Centinel Spine

Product Labels: Spinal Fusion

Tags: 510(k) Clearance, Regulatory