SAN JOSE, Calif., April 20, 2016 /PRNewswire/ -- SI-BONE, Inc., a medical device company that pioneered the use of the iFuse Implant System® ("iFuse"), a minimally invasive surgical (MIS) device indicated for fusion for certain disorders of the sacroiliac (SI) joint, announced the publication of two-year results from SIFI (Sacroiliac Joint Fusion with iFuse Implant System) a prospective multicenter clinical trial of SI joint fusion. The trial included 172 subjects at 26 US centers and was published in The International Journal of Spine Surgery which is the official journal of the International Society for the Advancement of Spine Surgery (ISASS). The publication is titled Triangular Titanium Implants for Minimally Invasive Sacroiliac Joint Fusion: 2-Year Follow-up from a Prospective Multicenter Trial and the lead author was Bradley Duhon, MD of the University of Colorado.i
Figure 1 - VAS SI Joint Pain
Figure 2 - Oswestry Disability Index (ODI)
About SI-BONE, Inc.
SI-BONE, Inc. (San Jose, California) is a leading sacroiliac joint medical device company dedicated to the development of tools and products for patients with low back issues related to certain SI joint disorders. The company develops, manufactures and markets minimally invasive products for the SI joint. SI-BONE, Inc. received original 510(k) clearance in November 2008 from the Food and Drug Administration (FDA) to market its iFuse Implant System. The CE mark for European commercialization was obtained in November 2010.