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SACRIX

LEAST
Less Exposure Advanced Spine Technologies

Incidence
22%
of patients with low back pain and 43% with prior lumbar fusion suffer from SI Joint Pain

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Sacroiliac Joint Fixation

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Sacrix invented the 100% fluoroscopic percutaneous lateral-oblique sacroiliac joint fusion technique and patented the titanium implant technologies. 

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FDA-Approved since 2015

Indications For Use

The Sacrix® Sacroiliac Joint Fusion Device System is indicated for transfixation of the sacroiliac joint to achieve fusion for conditions including sacroiliac joint disruptions and degenerative sacroiliitis.

AVOIDS THE GLUTEAL MUSCLES, NERVES AND VESSELS

SACRIX FEATURES

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COMPETITION

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TECHNIQUE

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PRODUCT CATALOG

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CODING & BILLING

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CASES
0% Device failure or loosening of Sacrix

UNILATERAL

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Adjacent SIJ breakdown after lumbar fusion

BILATERAL

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SUPPORTING ILIAC SCREWS

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SUPPORTING ILIAC SCREWS

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SACROPLASTY

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AVOID DOING THESE CASES

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Direct posterior intra-articular implants are unknowingly misplaced into the sacrum or ilium, only seen on CT scans

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Study shows you need three implants for direct lateral SIJ, not two

REVISIONS

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Revision Failed Direct Lateral SI-BONE iFuse Wedges

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Revision Failed Direct Lateral Genesys SIros Screws

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