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Every aspect of StabiLink was engineered to address the gap between conservative care and more invasive spinal fusion procedures — built on real-world evidence.
Engineered to provide supplemental fixation while supporting bony fusion.
Independent review of CT-assessed cases. Data on file, Southern Spine, LLC.
Designed to engage the lamina for enhanced stability.
A less invasive posterior approach designed for quicker recovery potential.
Same-day discharge potential — designed for outpatient surgical workflows.
Cleared for single-level use as a posterior, non-pedicle supplemental fixation device.
A decade-plus of real-world surgical use and refinement.
A supplemental approach that doesn't preclude escalation if ever needed.
Training and onboarding support provided to qualified clinicians.
A decade-plus of real-world surgical use by spine surgeons performing supplemental interlaminar fixation — across community hospitals, academic centers, and ASCs.
The StabiLink® Interlaminar Fixation System was developed by Hugh F. Smisson III, MD, a practicing neurosurgeon who saw a gap in the operating room — patients who needed more than a decompression alone, but not the disruption of a full pedicle screw construct. What began as one surgeon's solution has since been used in more than 7,000 procedures, refined and improved along the way.
Southern Spine has spent a considerable amount of time perfecting StabiLink's "one of a kind" laminar fixation design, manufacturing, and surgical technique — building a clinical track record that includes independent CT review showing 90%+ verified fusion.* Now, with more than a decade of real-world use behind it, StabiLink is being brought to a broader market of physicians and patients nationwide.
Southern Spine is an ISO 13485:2016 certified manufacturer focused on delivering safe, efficient, and reliable solutions that support improved outcomes for surgeons and patients.
*90%+ CT-verified fusion — data on file, Southern Spine.
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