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SI-BONE, Inc. Announces Spring Society Meeting Attendance
Date:3/4/2013

the end of April, the company will exhibit at the AANS meeting in New Orleans, LA from April 29th through May 1st in booth #1142.  During the meeting, Dr. Donald Sachs will present his clinical outcomes with iFuse during a poster session.  Mr. Dunn commented: "These next few months provide a great opportunity for us to support these key societies and continue our mission to educate and collaborate with their membership on advancing the diagnosis and treatment of patients who suffer from SI joint disorders."

SI-BONE, Inc. received original clearance in November 2008 from the Food and Drug Administration (FDA) to market its iFuse Implant System for fracture fixation of long bones and large bone fragments of the pelvis for conditions including sacroiliac joint disruptions and degenerative sacroiliitis, and an additional clearance in April 2011 for sacroiliac joint fusion for conditions including sacroiliac joint disruptions and degenerative sacroiliitis. The CE mark for European commercialization was obtained in November 2010.

Clinical publications have identified the SI joint as a pain generator for up to 22% of low back pain patients.4  In addition, DePalma et al, Pain Medicine 2011, identified the SI joint as a pain generator in low back pain in 40 to 61% of post-lumbar fusion patients, so-called "failed back surgery" patients.5  Initial treatment options for patients with SI joint disorders typically involve non-surgical management and, when non-surgical treatment of the SI joint fails, surgical treatments such as the iFuse may provide an option.

The iFuse Implant System is a commercially available device in the U.S. and Europe.   The iFuse procedure uses a small inci
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SOURCE SI-BONE, Inc.
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