iFuse TORQ TNT™ Implant System

Pelvic Bone Density-Driven Design

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").

 

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 osseointegration3

TORQLock™ Threads Hooked Profile

Designed to reduce toggle

FDA Breakthrough Device Designation

The FDA determined iFuse TORQ TNT has the potential to provide more effective fixation of pelvic fragility fractures than the current standard of care, cannulated screws.

  • 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 osseointegration3
  • TORQLock™ Threads Hooked Profile Designed to reduce toggle
  • FDA Breakthrough Device Designation The FDA determined iFuse TORQ TNT has the potential to provide more effective fixation of pelvic fragility fractures than the current standard of care, cannulated screws.

Bone Density-Driven Design 

Designed to reduce loosening through pelvis-specific fixation.
Variable thread heights and leads tailored to the posterior pelvis.

References

  1. Bone density mapping based on 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.
  2. Gardner 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
  3. SI-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.)
  4. SI-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./

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