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# Elaris Pedicle Screw System Cleared
- URL: https://www.fdaweb.com/elaris-pedicle-screw-system-cleared/
- Published: 2019-08-13T12:00:00.000Z
- Updated: 2026-09-15T01:43:23.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5144761

FDA has cleared a SpineWelding 510(k) for its Elaris Pedicle Screw System, which is intended to provide immobilization and stabilization of spinal segments through posterior, non-cervical, pedicle fixation in skeletally mature patients as an adjunct to fusion. The device is indicated for use in treating degenerative disc disease, spondylolisthesis, spinal stenosis, curvatures, tumor, pseudarthrosis, and a failed previous fusion. It discharges a liquid polymer that solidifies immediately upon contact with bone, “forming a confined, solid ring around the tip of the screw,” the company says.