Kleiner Device Labs Receives FDA Market Clearance for KG2 Surge Flow-Thru Interbody System

September 22, 2021 — Incline Village, Nev., — Kleiner Device Labs today announced that it has received U.S. Food and Drug Administration (FDA) 510(k) market clearance for its KGTM2 SurgeTM flow-thru interbody system. The system maximizes total bone graft delivery volume, better distributes graft bilaterally into the intervertebral disc space, and streamlines the implant delivery, […]