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# Centinel Spine Interbody Fusion Devices Cleared
- URL: https://www.fdaweb.com/centinel-spine-interbody-fusion-devices-cleared/
- Published: 2018-06-11T12:00:00.000Z
- Updated: 2026-09-15T00:12:06.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5141653

FDA has cleared a Centinel Spine 510(k) to market its FLX Platform of integrated interbody and non-integrated interbody fusion devices. The 3D-printed, all-titanium devices feature a combination of solid and porous radiolucent sections designed to reduce mechanical stiffness and improve visibility, compared to solid titanium implants, according to the company. The devices also feature a proprietary Fuse-Thru trabecular scaffold, designed to allow for bony in-growth and on-growth throughout the implant, the company says.