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The Vulcan Spinal System is intended for posterior, non-cervical, pedicle fixation as an adjunct to fusion for the following indications: degenerative disc disease (DDD - defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e. fracture or dislocation), spinal stenosis, curvatures (i.e. scoliosis, kyphosis, or lordosis), tumor, pseudarthrosis, and/or failed previous fusion.

When used for posterior non-cervical pedicle screw fixation in pediatric patients, the Vulcan Spinal System implants are indicated as an adjunct to fusion to treat progressive spinal deformities (i.e., scoliosis, kyphosis, or lordosis) including idiopathic scoliosis, neuromuscular scoliosis, and congenital scoliosis. Additionally, the Vulcan Spinal System is intended to treat pediatric patients diagnosed with: spondylolisthesis/spondylolysis, fracture caused by tumor and/or trauma, pseudarthrosis, and/or failed previous fusion. This system is intended to be used with autograft and/or allograft. Pediatric pedicle screw fixation is limited to a posterior approach.

Refer to the Compatibility section of the VB Spine Vulcan Spinal System Instructions for Use for a listing of compatible systems.

The Vulcan Spinal System is a top-loading, multiple component, non-cervical spinal fixation system implanted from the posterior approach and designed to provide fixation during the fusion process. The system is composed of polyaxial pedicle screws, locking set screws, and rods.

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VB Spine Q Interbody Instruments are intended to be used as accessories to Stryker's Spine Guidance System to facilitate placement of VB Spine implants. They can be navigated instruments or non-navigated manual instruments. When navigated, VB Spine Q Interbody Instruments are specifically designed for use with Stryker's Spine Guidance Software. They are intended to be used with associated trackers and adaptors to facilitate preparation and placement of VB Spine interbody implants in accordance with the indications and contraindications of the associated VB Spine Implant System and/or Stryker's Spine Guidance System.

The Q Interbody Instruments include Q Inserters and Q Interbody Trials, as well as new system components including Q Calibration Devices. The Q Interbody Instruments are intended to be used to facilitate preparation and placement of VB Spine interbody implants.

These instruments are designed to be compatible with Stryker's Spine Guidance 5.3 Software.

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