Designed With A Purpose

Pedicle Screw System is a cannulated system for MIS, LES and open procedures. Its set screw and tulip have a reverse thread that resists cross threading and creates a lock between the tulip and set screw to virtually eliminate splay.

Key Features
  • Cannulated system for MIS, LES and Percutaneous procedures
  • Up to 60° of polyaxial rotation can be achieved between tulip and screw
  • Color-coded implants for ease of identification
  • Re-animation of tulip after final locking and unlocking of system
  • Friction fit washer maintains tulip position
  • Tulip lead-in for set screw to minimize cross-threading
  • Reverse thread resists cross-threading and creates a lock between tulip and set screw, virtually eliminating splay
INDICATIONS
The SpineFrontier® PedFuse® Pedicle Screw System is intended to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute instabilities or deformities of the thoracic, lumbar, and sacral: degenerative spondylolisthesis with objective evidence of neurological impairment, fracture, dislocation, scoliosis, kyphosis, spinal tumor, and failed previous fusion (Pseudarthrosis).
In addition, the SpineFrontier® PedFuse® Pedicle Screw System is indicated for the treatment of severe spondylolisthesis (Grade 3 and 4) of the L5-S1 vertebra in skeletally mature patients receiving fusion by autogenous bone graft, with the device fixed or attached to the lumbar and sacral spine. When used in a percutaneous approach with MIS instrumentation, the SpineFrontier® PedFuse® Pedicle Screw System is intended to provide immobilization and stabilization of spine segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute instabilities or deformities of the thoracic, lumbar and sacral spine: degenerative spondylolisthesis with objective evidence of neurological impairment, fracture, dislocation, scoliosis, kyphosis, spinal tumor, failed previous fusion (Pseudarthrosis) and severe spondylolisthesis (Grade 3 and 4) of the L5-S1 vertebra in skeletally mature patients receiving fusion by autogenous bone graft, with the device fixed or attached to the lumbar and sacral spine.