Designed With A Purpose

The MISquito MIS technique, used in conjunction with the PedFuse® Respond® Pedicle Screw System, is a method for percutaneously delivering a pedicle screw and rod construct. MISquito’s innovative rod guidance system allows surgeons to control and guide both ends of the rod as it is inserted into its optimal position.

Key Features
  • Instrumentation is compatible with PedFuse REspond System
  • Screw and portal constructs allow smaller incisions for patients
  • Bulleted rod for accurate and smooth insertion
  • Innovative method which utilizes proprietary technology to guide rods into desired location
  • Rod control is maintained per current technique standard
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.