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# FDA Clears Aurora Spine Cervical Plate
- URL: https://www.fdaweb.com/fda-clears-aurora-spine-cervical-plate/
- Published: 2021-03-25T12:00:00.000Z
- Updated: 2026-09-14T16:52:13.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5148976

FDA has cleared an Aurora Spine 510(k) for its proprietary Apollo Anterior Cervical Plate system, featuring a 1.9mm design with hyper-angulation variability in the Cephalad Caudal and screw angulation of 32 degrees. The company says the device is designed to help reduce common postoperative complications — such as dysphagia, malalignment, and adjacent level ossification — by enabling surgeons to customize treatment to patient needs versus a traditional one-size-fits-all approach. It also features **implant length options** to match a variety of patient anatomies, and s**crew offerings** with fixed and variable angles to enable better screw placement and locking accuracy, the company says.