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# FDA Clears 4Web Lumbar Interbody Fusion Device
- URL: https://www.fdaweb.com/fda-clears-4web-lumbar-interbody-fusion-device/
- Published: 2020-06-10T12:00:00.000Z
- Updated: 2026-09-14T16:17:46.000Z
- Author: David McFarland
- Tags: Drugs, #legacy-id-D5146971

FDA has cleared a 4Web Medical 510(k) to market its Stand-Alone Anterior Lumbar Interbody Fusion Device. It is designed to allow fixation screws to be placed through the truss implant and into the adjacent vertebral bodies creating a zero-profile stand-alone construct that removes the need for supplemental fixation, the company says. Additionally, the device features single-step locking mechanisms and it is available in sterile packaging in multiple footprints, lordotic angles, and heights, it says.