Elevation Spine Receives FDA 510(k) Clearance for Saber-XA™, an Expandable Anterior Lumbar Interbody Fusion (ALIF) System
Elevation Spine announced today that the U.S. Food and Drug Administration (FDA) has granted 510(k) clearance for Saber-XA™, an anterior lumbar interbody fusion (ALIF) system that combines expandable cage technology with a zero-profile, FDA-cleared anterior lumbar plate. Saber-XA expandable technology enables true intra-operative customization of implant height and lordosis.
Elevation Spine Receives FDA 510(k) Clearance for Saber-C® AVIA™, A Complete Anterior Cervical Fixation System with a Porous 3D-Printed Titanium Interbody
Elevation Spine today announced that the U.S. Food and Drug Administration (FDA) has granted 510(k) Clearance for Saber-C® AVIA™, the newest product line in the Saber platform. Saber-C AVIA is engineered as a zero-profile anterior cervical discectomy and fusion (ACDF) construct with the biomechanical stability historically associated with traditional plating and features a porous 3D-printed titanium interbody with both spike and screw fixation options.
Elevation Spine Surpasses 5,000 Saber-C® Implantations, Marking a Significant Milestone for Its Integrated Cervical Fixation Platform
Elevation Spine announced today that its Saber-C Anterior Cervical Fusion System has surpassed 5,000 implantations, a milestone that reflects growing surgeon adoption of its proprietary integrated-fixation approach to anterior cervical discectomy and fusion (ACDF). The Saber-C system combines the stability of traditional anterior cervical plating with the streamlined workflow of a zero-profile interbody construct through its proprietary Saber™ in-line spike fixation technology.
