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# FDA Clears K2M Yucon Spinal System
- URL: https://www.fdaweb.com/fda-clears-k2m-yucon-spinal-system/
- Published: 2017-09-29T12:00:00.000Z
- Updated: 2026-09-14T22:53:22.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5139749

FDA has cleared a K2M Group Holdings 510(k) for its [Yukon Oct Spinal System](https://www.globenewswire.com/Tracker?data=cOudan9mdjRtWKuzl4LuwkZQ7N8YDzKPGw6BlHXRaZV3qVJ40HS8SQYXSYSkO-ZBH7NcBJzTDh%5FPF6iOyBtqbG6giCe-VmhInmVrAPBlIQQVH2%5FSXcRDITyl8IW0fPvL&ref=fdaweb.com), a device intended to facilitate fusion with posterior fixation in the occipito-cervico-thoracic regions of the spine. The device features “newly designed top-loading, high angulation, polyaxial screws that provide up to 105 degrees of polyaxial angulation,” the company says. Its screw heads accept both 3.5 and 4.0 mm rods in both cobalt chrome and titanium, and accommodate construct rigidity based on degenerative or deformity corrections, it says.