The Minuteman® is a minimally invasive, interspinous-interlaminar fusion device intended for the fixation and stabilization of the thoracic, lumbar, and sacral spine while awaiting bony fusion to occur The Minuteman® is designed for attachment to the posterior non-cervical spine at the spinous processes through its bilateral locking plates, and it is intended for use with bone graft material placed within the device. It provides immobilization and stabilization of the spinal segments. The core threaded post allows for optimal placement and a wide range of sizes allows for enhanced anatomical fit. The Minuteman® is delivered sterile and individually packed.
Features & Benefits
Minimally Invasive – Alternative to traditional pedicle screws and other spinous process plates
Low Profile – With 12mm removable portion of the implant body
Ligament Preservation – Of the supraspinous ligament helps maintain stabilization of the spine
Lateral MIS Approach – Eliminates the lateral dissection of the healthy tissue (neural monitoring is not required)
5 Anatomical Sizes – (8mm, 10mm, 12mm, 14mm, and 16mm) to accommodate variations in patient anatomy
Safer Zone – Lateral MIS approach is above the facet joints, avoiding the neural and vascular structures
Threaded Body – Allows the implant to thread between the spinous processes in a controlled fashion
Hydroxyapatite Coating – Naturally occurring substance that helps promote bone on-growth and fusion
Large Graft Window – Allows easy placement of bone graft material to facilitate a posterior fusion
Sterile Packed – Promotes patient safety and compliance at hospitals
Reversible Auto-Lock – Enables the device to variably tighten without compromising fixation
Indications for Use
The Minuteman® MIS Fusion Plate is a posterior, non-pedicle supplemental fixation device, intended for use at a single level in the non-cervical spine (T1-S1). It is intended for use with bone graft material and is not intended for stand-alone use. The Minuteman® MIS Fusion Plate may be implanted via a minimally invasive lateral (L1-S1) approach. It is intended for plate fixation/attachment to spinous processes for the purpose of achieving supplemental fusion in the following conditions: Lumbar Spinal Stenosis, Degenerative Disc Disease, Spondylolisthesis, Trauma, and Tumor.
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Disclaimer: Our health care practitioners perform one or more regenerative therapies that have not yet been approved by the United States Food and Drug Administration. The use of these products is experimental and investigative. Any patient testimonials found on our website or other web properties should not be interpreted as a statement on the effectiveness of any of our medical treatments.