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# Aurora Spine SiLO Sacroiliac Device Cleared
- URL: https://www.fdaweb.com/aurora-spine-silo-sacroiliac-device-cleared/
- Published: 2022-10-06T12:00:00.000Z
- Updated: 2026-09-14T18:02:08.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5152911

FDA has cleared an Aurora Spine 510(k) for its SiLO TFX MIS Sacroiliac Joint Fixation System. The device is intended for conditions including sacroiliac joint disruptions and degenerative sacroiliitis, according to the company. Comprising a transfixing-cone, an ilium screw, a sacrum screw and associated instrumentation, the device is designed to transfix the sacrum and ilium to provide stability for bony fusion, it says.