Anterior Cervical PlateThe Spine360 design features a thin profile with large graft windows enhancing visualization and minimizing tissue damage enhancing faster recovery. Designed with a small degree of lordosis and enhanced load sharing that promotes fusion. Anterior Cervical Plates are offered in 1, 2, 3, and 4 level sizes. FDA approved Spine 360 Anterior Cervical Plate System is intended for anterior screw fixation to the cervical spine (C2-C7) as an adjunct to fusion in the treatment of the following:
Talon Spinal Fixation SystemSpine360’s Talon system features an anti-cross threading locking plug assembly that expedites the insertion of the locking plug while reducing splaying and misplacement of the locking plug. A double lead screw thread allows of a fast screw insertion and great pull out strength while maximizing fatigue strength. The Talon Low Top and High Top design features a friction head that enables quick and simple construct assembly. The low profile design provides extra space for graft with minimal above rod protrusion. The polyaxial head allows for maximum angulation and reduces the need for rod contouring. The Talon High Top Design features a longer tulip which aides in rod reduction; the longer tulip is designed with a break-off feature for a low profile finish. The Talon Spinal System including 4.5, 5.0, 6.0, 7.0 and 8.0mm diameter pedicle screw assemblies, 5.0 rods and 3 sizes of cross-links are approved by the FDA as 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 and chronic instabilities or deformities of thoracic, lumbar, and sacral spine: severe spondylolisthesis (grades 3 and 4) of the L5-S1 vertebra; degenerative spondylolisthesis with objective evidence of neurologic impairment; fracture; dislocation; scoliosis; kyphosis; spinal tumor; and failed previous fusion (pseudoarthrosis).
Minimally InvasiveSpine360 has evolved innovative cannulated instrumentation and implants technology in the Serpent product line that provides new excellent product features such as aggressive screw insertion with less turns required and maximizing fatigue strength and pullout strength. The Serpent is designed with a screw extension tower, no separate tower or blades are required to assemble or disassemble. An incorporated ring located at the top of the tower eliminates splaying of the tower during use and allowing smooth insertion of the locking plug. The Talon Spinal System is approved by the FDA as 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 and chronic instabilities or deformities of thoracic, lumbar, and sacral spine: severe spondylolisthesis (grades 3 and 4) of the L5-S1 vertebra; degenerative spondylolisthesis with objective evidence of neurologic impairment; fracture; dislocation; scoliosis; kyphosis; spinal tumor; and failed previous fusion (pseudoarthrosis). The minimally invasive surgical technique is FDA approved.
Peek ProductsManufactured from Invibio PEEK-Optima® Spine360 has:
Featuring large graft windows and superior configurations that prevent migration and provide ease of insertion. The Spine 360 Lumbar Cages are approved by the FDA as indicated for intervertebral body spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) at one level from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by patient history and radiographic studies. These DDD patients may also have up to Grade I spondylolisthesis or retrolisthesis at the involved level. Spine 360 Lumbar Cages implants are to be used with autogenous bone graft and implanted via a posterior, transforaminal or anterior approach. The Spine 360 Lumbar Cage is to be used with supplemental fixation.
Buttress SystemThe Black Widow buttress plate and buttress plate screw are made of Titanium Alloy (TI 6AI-4V ELI). TI 6AI-4V ELI was chosen because of its excellent biocompatibility, good fatigue strength, and low elastic modulus which is similar to that of bone or other biocompatible materials. The FDA approved Black Widow Anterior Buttress Plate, in conjunction with traditional rigid fixation, is intended for use in spinal fusion procedures as a means to maintain the relative position of weak bony tissue such as allografts or autografts. View Our Products |
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