CoreLink Gains FDA Clearance for Foundation 3D ALIF

By Julie A. Vetalice

CoreLink received FDA 510(k) clearance to market the Foundation™ 3D Anterior Lumbar Interbody Fusion (ALIF) device. This builds on the company's Foundation 3D cervical, curved lumbar and straight lumbar devices, which were fully launched as of early 2Q18.

The devices are based on proprietary Mimetic Metal™ technology that is designed to mimic key characteristics of natural bone, and feature StrutSure™ technology that combines load-sharing support and an interconnected lattice for balanced strength, stiffness and stability.

Sources: CoreLink, LLC; ORTHOWORLD Inc.

CoreLink Foundation 3D ALIF

Image courtesy of CoreLink

Product Labels: Spinal Fusion

Tags: 510(k) Clearance, Regulatory