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# ChoiceSpine 510(k) for Cervical Spacer System
- URL: https://www.fdaweb.com/choicespine-510-k-for-cervical-spacer-system/
- Published: 2021-05-25T12:00:00.000Z
- Updated: 2026-09-14T17:00:17.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5149401

FDA has cleared a ChoiceSpine 510(k) for the Blackhawk Ti Cervical Spacer System. The 3D-printed device is made using the company’s BioBond porous titanium technology, according to ChoiceSpine. It also features a large open graft window for bone graft containment and maximum visualization, and a simultaneous, single-step anchor deployment. Blackhawk is available in six degree lordotic and convex configurations.