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# FDA Clears Camber Spine’s Interbody Fusion Implant
- URL: https://www.fdaweb.com/fda-clears-camber-spines-interbody-fusion-implant/
- Published: 2017-08-15T12:00:00.000Z
- Updated: 2026-09-14T22:41:11.000Z
- Author: David McFarland
- Tags: Drugs, #legacy-id-D5139382

FDA has cleared a Camber Spine Technologies 510(k) for the SPIRA Open Matrix ALIF device, an interbody fusion implant consisting of spiral support arches and the company’s “Surface by Design” technology.“The spiral support arches decrease subsidence by load sharing over the entire endplate, while also maximizing bone graft capacity,” the company says. The Surface by Design technology is a deliberately designed roughened surface that is intended to promote bone growth through an optimized pore diameter, strut thickness and trabecular pattern, it adds. The device is indicated for use in skeletally mature patients with degenerative disc disease at one or two contiguous levels from L2-S1\. It is intended to be used with additional FDA-cleared supplementary fixation systems.