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# FDA Clears joimax Spinal Cages
- URL: https://www.fdaweb.com/fda-clears-joimax-spinal-cages/
- Published: 2021-09-08T12:00:00.000Z
- Updated: 2026-09-14T17:13:30.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5150101

FDA has cleared a joimax 510(k) for the EndoLIF Delta Cage and EndoLIF DoubleWedge Cage, intended for intervertebral body fusion procedures for various diseases of the lumbar spine, such as degenerative disc disease. The 3D printed titanium products are designed for bone ingrowth, and are fillable with bone or bone substitute material, pre- or post-insertion, according to the company. They also feature “over-the-wire” implantation for improved targeted positioning in the intervertebral disc space, it says.