Designed With A Purpose

The PedFuse REspond X Pedicle Screw System is a cannulated system for LES and percutaneous procedures. It's Innovative method which utilizes proprietary technology to guide rods into desired location.

Key Features
  • Screw and portal constructs allow smaller incisions for patients
  • 60° of polyaxial rotation can be achieved between tulip and screw
  • Color-coded implants for ease of identification
  • Bulleted rod for accurate and smooth insertion
  • 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
  • Innovative method which utilizes proprietary technology to guide rods into desired location
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.