Elevation Spine lands FDA clearance for expandable interbody fusion system

Elevation's FDA clearance for Saber-XA follows the agency's clearance of its Saber-C AVIA cervical fixation device in July.

Elevation Spine has obtained US Food and Drug Administration (FDA) clearance for Saber-XA, an anterior lumbar interbody fusion (ALIF) system with an expandable cage for degenerative disc disease treatment and spinal column stabilisation.

Elevation highlighted that due to Saber-XA’s form factor, surgeons can independently adjust the implant’s height angle based on individual patient anatomy.

FDA clearance for Saber-XA comes weeks after the California-based company secured FDA clearance for Saber-C AVIA, a cervical fixation device to treat spinal pathologies including nerve compression by stabilising the vertebrae, damaged disc replacements, and to promote bone fusion.

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