Leverage the iFuse Neuromonitoring Kit to identify spinal nerve roots during iFuse Procedure.SM
View a three-dimensional representation of the lumbar spine, sacrum, and ilium. Red dashed outlines depict common positioning of three iFuse Implants™ across the sacroiliac joint. Of the neural structures shown, the L5, S1, and S2 nerves (labeled in the figure) are at greatest risk of injury during such procedures.1
GUIDE PIN SLEEVE
GUIDE PIN CAP AND GUIDE PIN CLIP
MONOPOLAR PROBE
This 3 minute video shows how the iFuse Implants are used in minimally invasive SI joint fusion surgery.
View other videosMedical professionals can order the iFuse-Neuromonitoring Kit by contact your local SI-BONE sales representative or by calling SI-BONE at:
PH 408.207.0700 or contact sales@si-bone.com
References
1. Woods et al. “Utility of Intraoperative Neuromonitoring during Minimally Invasive Fusion of the Sacroiliac Joint”, Advances in Orthopedics, Vol 2014, Article ID 154041.
2. Versus makeshift solutions
3. Guide Pin Cap is designed for use with 3.2mm Guide Pins only
4. Do not place probe through cannula of 4mm iFuse Implant™
The Neuromonitoring Kit is indicated for stimulation of peripheral motor nerves, including spinal nerve roots, for localization and identification during surgery.
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 and Neuromonitoring Kit. 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.
U.S. Patent Nos. 8,202,305; 8,840,623; 8,986,348 and 9,039,743; pending U.S. and foreign patent applications
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