Diagnosing SI joint pain includes a physical exam of the SI joint, spine, hips and pelvis, provocative tests, and diagnostic injections.
Are You a Provider?The iFuse triangle-shaped implant has been designed specifically for the SI joint.
Are You a Provider?The iFuse Implant, first 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 1 randomized controlled trials (RCTs).
Are You a Provider?As with other joints in the body, the SI joint can become damaged from trauma, degeneration and everyday wear and tear.
Are You a Provider?W. Carlton Reckling, MD* discusses his personal iFuse Case Series
*Dr. Reckling is the Vice President of Medical Affairs at SI-BONE, Inc.
The iFuse Implant System is intended for sacroiliac fusion for conditions including sacroiliac joint dysfunction that is a direct result of sacroiliac joint disruption and degenerative sacroiliitis. This includes conditions whose symptoms began during pregnancy or in the peripartum period and have persisted postpartum for more than 6 months. There are potential risks associated with the iFuse Implant System. It may not be appropriate for all patients and all patients may not benefit. For information about the risks, visit: www.si-bone.com/risks
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