iFuse TORQ TNT™
Pelvic Bone Density-Driven Design1
iFuse TORQ TNT™ Implant: the first 3D-printed, porous, threaded implant with lengths capable of spanning the posterior pelvis, passing through the ipsilateral ilium, sacrum, and through the contralateral ilium (through and through, "TNT").
Features
- Pelvis-Specific 8.7 mm Diameter Fits 95% of S1 corridors suitable for a 7.3 mm transsacral screw2. 150% stronger in bending vs 7.3 mm stainless steel screw3, 4
- FuSlon 3D™ Surface 3D Printed Porous Lattice Designed for osseointegration5
- Self-Drilling, Self-Tapping Decreases surgical steps
- TORQLock™ Threads Hooked Profile Designed to reduce toggle
Designed to reduce loosening through pelvis-specific fixation. Variable thread heights and leads tailored to the posterior pelvis.
Case Studies
It is one of the most gratifying procedures that I actually perform in spine surgery. It's truly been a change for my practice, for the good.”
Douglas Kasow, DO
Board Certified Orthopedic Spine Surgeon
Piedmont Orthopedics Ortho Atlanta
Professional Training
1Thread pitch and surface design of iFuse TORQ TNT are based on variable Thread pitch and surface design of iFuse TORQ TNT are based on variable bone density in the pelvis as documented by Thiesen DM, et al. The three-dimensional bone mass distribution of the posterior pelvic ring and its key role in transsacral screw placement. Sci Rep. 2020 Mar 30;10(1):5690.
2Gardner MJ, et al. Quantification of the upper and second sacral segment safe zones in normal and dysmorphic sacra. J Orthop Trauma. 2010 Oct;24(10):622-9. —Data analyzed for S1 dimensions
3SI-BONE Technical Study 301122-TS-A. Fatigue Testing of 7.3mm Fully Threaded Cannulated Screw. (Mechanical data, including computational modeling, is not necessarily indicative of human clinical outcomes.)
4SI-BONE Test Report 301321-R-A. Static and Dynamic Cantilever (ASTM F2193) Testing of the iFuse TORQ TNT Implants. (Mechanical data, including computational modeling, is not necessarily indicative of human clinical outcomes.
5SI-BONE Technical Study 301067-TS-A. iFuse Implant Osseintegration Claim Technical Study.
Healthcare professionals should refer to the Instructions For Use for indications, contraindications, warnings, and precautions at https://ous.si-bone.com/label.
There are potential risks associated with iFuse procedures. They may not be appropriate for all patients and all patients may not benefit.
For information about the risks, visit https://ous.si-bone.com/risks.






