Aurora Spine Corporation announced it has received 510(k) clearance from the United States Food and Drug Administration FDS for the patented minimally invasive SiLO TFX MIS Sacroiliac Joint Fixation System. The Aurora Spine SiLO TFX MIS Sacroiliac Joint Fixation System, is intended for sacroiliac joint fusion for conditions including sacroiliac joint disruptions and degenerative sacroiliitis. The SiLO TFX MIS Sacroiliac Joint Fixation System includes a Transfixing-Cone, an ilium screw, a sacrum screw and associated instrumentation.

The SiLO TFX implants are designed to transfix the sacrum and ilium, providing stability for bony fusion.