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Aurora Spine Corporation Announces FDA 510(k) Clearance for its SiLO TFX™ MIS Sacroiliac Joint Fixation System

Aurora Spine Corporation Announces FDA 510(k) Clearance for its SiLO TFX™ MIS Sacroiliac Joint Fixation System
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Aurora Spine Corporation Announces FDA 510(k) Clearance for

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Aurora Spine receives lumbar spinal stenosis indication for minimally invasive implants

Aurora Spine Corporation has announced FDA clearance of a new lumbar spinal stenosis indication for use with Aurora’s ZIP platform of minimally invasive spine surgery implants, according to a press release.Other FDA-cleared indications for use of the ZIP minimally invasive (MIS) interspinous fusion system include degenerative disc disease, spondylolisthesis, trauma and tumors.

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