Meet Patients Who Chose the iFuse Implant System®
Minimally Invasive Sacroiliac Joint Surgery
Meet seven patients who suffered with sacroiliac joint disorders; a challenging condition affecting upwards of 25% of patients with axial low back pain.1 Talk with a specialist to find out if your low back problems are caused by a sacroiliac joint problem, and if the iFuse Implant System is an appropriate option for you.
This information is not intended to take the place of a doctor's advice. Please keep in mind that treatment and outcome results vary among patients. 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. Clinical studies have demonstrated that treatment with the iFuse Implant System improved pain, patient function, and quality of life at 12 months post-implantation. 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, read the Important Safety Information.