SI-BONE is focused on educating patients and providers on one of the most under-diagnosed and under-treated areas in spine, the sacroiliac (SI) joint.
The iFuse Implant, cleared by the FDA in 2009, is the only device for treatment of SI joint dysfunction that is supported by significant published clinical evidence, including two Level I Randomized Controlled Trials (RCTs).
The clinical evidence shows safety, durable effectiveness, and lasting relief from SI joint pain.
The SI joint is located in the posterior pelvis, linking the iliac bones (pelvis) to the sacrum (lowest part of the spine above the tailbone).
The function of the SI joint is to transfer body weight and forces from your upper body through the pelvis to your legs and vice versa. The SI joint plays a crucial role in absorbing shocks, which prevents impact forces during activity from reaching the spine.
Similar to other joints in the body, the SI joint is susceptible to injury, degeneration, inflammation or arthritis, which may result in dysfunction. When this happens, you may feel pain in your buttock and sometimes in the lower back and legs, especially when running, walking, lifting or even lying on the affected side.
SI-BONE’s iFuse Implant System was designed for minimally invasive SI joint fusion. Through a small ~3 cm incision, typically 3 triangular titanium implants are inserted in a lateral to medial orientation across three dense cortical bone walls (ilium outer, ilium inner, and sacrum outer).
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