Kleiner Device Labs Gets 510(k) Clearance for KG2 Surge Flow-Thru Interbody System

Kleiner Device Labs has received the FDA’s 510(k) clearance for its KG2 Surge flow-thru interbody system for spinal fusion. 

The KG2 Surge system comes with a pre-assembled 3-D printed titanium device that features a diamond lattice porous structure that helps promote bone ingrowth.

The system allows surgeons to pack the intervertebral disc space with graft material using a rectangular tube that “allows simplified delivery of a wide range of allograft and autograft products, including viscous and fibrous materials,” the company says.