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Coflex® Interlaminar Technology

Front Range Center for Brain & Spine Surgery uses coflex® Interlaminar Technology, the first and only motion preserving minimally invasive treatment approved for moderate to severe spinal stenosis after decompression.

The coflex® Interlaminar Technology is an Interlaminar Stabilization® device indicated for use in one or two level lumbar stenosis from L1-L5 in skeletally mature patients with at least moderate impairment in function, who experience relief in flexion from their symptoms of leg/buttocks/groin pain, with or without back pain, and who have undergone at least 6 months of non-operative treatment.

The coflex® is intended to be implanted midline between adjacent lamina of 1 or 2 contiguous lumbar motion segments. The Interlaminar Stabilization® device is implanted after decompression of stenosis at the affected level(s). Please see Instructions for Use for complete list of warnings, precautions and contraindications.

Based on the FDA clinical study, when compared to the standard of care (fusion surgery), patients receiving the coflex® device experienced:

  • Shorter operating time and hospital stay
  • Quicker recovery
  • Faster and sustained pain relief
  • Greater mobility at treatment level
  • Natural movement at adjacent levels

 

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