Press release
SI-BONE, Inc. Announces that Updated ISASS Policy and Guidelines on MIS SI Joint Fusion Support Only Lateral Transiliac MIS Procedures
SANTA CLARA, Calif., Jan. 04, 2021 (GLOBE NEWSWIRE) -- SI-BONE, Inc., (Nasdaq: SIBN), a Silicon Valley-based medical device company dedicated to solving
About this update from Si-bone, Inc.
[{"type":"text","content":"SANTA CLARA, Calif., Jan. 04, 2021 (GLOBE NEWSWIRE) -- SI-BONE, Inc., (Nasdaq: SIBN), a Silicon Valley-based medical device company dedicated to solving musculoskeletal disorders of the sacropelvic anatomy, announced today that the International Society for the Advancement of Spine Surgery (ISASS) published an early view of its updated Policy on MIS Sacroiliac Joint Fusion (For Chronic Sacroiliac Joint Pain) in the December 2020 issue of the International Journal of Spine Surgery (https://www.ijssurgery.com). The policy and guidelines remain supportive of continued adoption of MIS SI joint fusion procedures by the clinician and payor communities, limited to procedures using a lateral transiliac approach, which includes the iFuse Procedure™. While the ISASS policy does not endorse any specific MIS SIJ system, the updated policy states that “…most high-level clinical evidence supporting the safety, effectiveness, durability and economic benefit of lateral MIS SIJF is derived from use of iFuse.” ISASS does not recommend MIS posterior (dorsal) SI joint fusion procedures, whether using an implantable device or a product such as bone allograft. This is due to the limited published clinical evidence supporting the safety and effectiveness of posterior (dorsal) SI joint fusion, as well as the key differences from lateral transiliac procedures such as the iFuse Procedure in terms of surgical steps, work effort and anatomy considerations. The ISASS policy states that the high-level clinical and safety data from evaluation of MIS lateral transiliac SI joint fusion devices such as iFuse “are likely not generalizable to these posterior (dorsal) MIS SIJF procedures.” W. Carlton Reckling, M.D., Chief Medical Officer and Vice President of Medical Affairs at SI-BONE, said “the updated ISASS policy and clinical guidelines provide important updates on the clinical evidence and the current medical practice including MIS SI joint fusion treatment options, which have evolved significantly over the past several years. The ISASS policy provides a roadmap and rationale for clinicians, payors and other third-party evaluators for their adoption of the iFuse Implant System.” About SI-BONESI-BONE is a medical device company that pioneered the iFuse Implant System, a minimally invasive surgical system for fusion of the sacroiliac joint to treat sacroiliac jo...