![FDA, FTC and DOJ Enforcement of Medical Device Regulations FDA, FTC and DOJ Enforcement of Medical Device Regulations](https://www.fdanews.com/ext/resources/Book-Covers-2/BFFDEMDR-COVER.png?height=200&t=1685733565&width=200)
Home » Kleiner Device Labs Gets 510(k) Clearance for KG2 Surge Flow-Thru Interbody System
Kleiner Device Labs Gets 510(k) Clearance for KG2 Surge Flow-Thru Interbody System
![ClearanceStamp_Orange.gif](https://www.fdanews.com/ext/resources/test/Device_Images6/ClearanceStamp_Orange.gif?t=1609798625&width=430)
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.
Upcoming Events
-
11Jul
-
18Jul
-
21Oct