FDAnews
www.fdanews.com/articles/209717-aurora-spine-received-510k-clearance-for-sacroiliac-joint-fixation-system

Aurora Spine Received 510(k) Clearance for Sacroiliac Joint Fixation System

October 10, 2022

Aurora Spine has received 510(k) clearance from the FDA for its SiLO TFX MIS sacroiliac joint fixation system.

The system is intended for sacroiliac joint fusion for conditions including sacroiliac joint disruptions and degenerative sacroiliitis. 

The system’s implants are designed to transfix the sacrum and ilium, providing stability for bony fusion. It includes a transfixing cone, an ilium screw, a sacrum screw and associated instrumentation.

The system offers a minimally invasive solution to treat sacroiliac joint disruption, a significant contributor to back pain, the company said.

View today's stories