> ## Content Index
> Fetch the complete content index at: https://www.fdaweb.com/llms.txt
> Use this file to discover other available public pages before exploring further.

# Providence Medical Tech Cavux Facet Device Cleared
- URL: https://www.fdaweb.com/providence-medical-tech-cavux-facet-device-cleared/
- Published: 2022-12-16T12:00:00.000Z
- Updated: 2026-09-14T18:10:05.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5153418

FDA has cleared a Providence Medical Technology Cavux Facet Fixation System (FFS) for spinal surgery patients requiring a revision for an anterior pseudarthrosis at one level, from C3 to C7, with autogenous and/or allogenic bone graft. FFS is an integrated cage and screw system that is implanted bilaterally in the facet joints to provide stabilization until fusion occurs.

The company says the clearance was based on data from the Providence-sponsored REVISE Clinical Study, which summarized real world evidence pooled across six clinical sites treating patients with the device to revise a prior anterior cervical discectomy and fusion.