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# FDA Clears K2M’s Ozark Cervical Plate Systems
- URL: https://www.fdaweb.com/fda-clears-k2ms-ozark-cervical-plate-systems/
- Published: 2018-06-07T12:00:00.000Z
- Updated: 2026-09-15T00:11:25.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5141631

FDA has cleared a K2M Group Holdings 510(k) for its Ozark Cervical Plate Systems for anterior screw fixation to the cervical spine (C2-T1) in patients with degenerative disease, deformity, tumor, or trauma. The systems are available in two designs, Ozark Guide and Ozark View, both featuring an advanced per-level, integrated locking cover that provides surgeons with clear visual and tactile confirmation of the final lock position, the company says. They both include a full range of plate and screw sizes and instrumentation for creating constrained, semi-constrained or hybrid screw constructs, it adds.