X-Spine Receives FDA 510(k) Clearance on AXLE Interspinous Fusion System

X-spine, a Miamisburg, Ohio-based global spine implant manufacturer, recently received FDA clearance on the AXLE interspinous fusion system, according to a company news release.

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The system is designed to provide spinal stability for lumbar fusion procedures, including treatment for degenerative disc disease, spinal tumors and trauma. The AXLE system includes an implant customized to conform to the patient’s anatomy that can be placed through a one-inch incision in the back.

The device attaches to the rearmost portion of the adjacent vertebrae of the lower spine.

Read the X-spine news release on AXLE.

Read more coverage on spinal systems:

– SpinalVu Begins Production on Cervical and Lumbar Interbody Systems

– Medtronic Receives FDA 510(k) Clearance for Spinal Cord Stimulator Trialing Cable

– Titan Spine Receives 510(k) Clearance on PLIF Device

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