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A Small Device with Big Potential for your Practice

VariLift®-LX is the only posterior stand-alone expandable lumbar interbody fusion device cleared by the FDA for 1 or 2 levels, PLIF or TLIF, with or without supplemental fixation, and intended for use with autograft and/or allograft tissue.

Zero Profile Construct Zero Profile Construct for True MIS, Outpatient or Inpatient

VariLift®-LX is a Zero-Profile, Minimally-Invasive Option for Patients with DDD, Grade 1 Spondylolisthesis, and Adjacent Segment Disease.

Graft Chamber_1 Large Graft Chamber allows Overpacking of Fusion Material

With 4 large fenestrations and a generous bone graft chamber, VariLift®-LX is designed to allow maximum contact between graft material and endplates.

Mechanical Strength Zero Mechanical Failures after 21k Implanted Devices

VariLift®-LX is made of titanium alloy (Ti-6Al-4V), a high-performance material well known for its strength and biocompatibility in orthopedic applications.1 

Non-Impact Insertion and Multi-Plane Expansion In Situ

Designed to Help Treat Collapsed Disc Spaces and Provide Immediate Stabilization

With a leading edge as small as 6mm, the VariLift®-LX enters into the disc space in a near cylindrical shape and expands in situ. The expansion causes the device edges to gain further purchase into the cortical endplates and provide immediate stability. 

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Generous Graft Chamber

Large Fenestrations for Fusion and Distribution of Bone Graft into the Disc Space

Once deployed, a large hollow inner chamber and wide fenestrations allow placement of local bone graft and ultimate growth of the intervertebral fusion throughout the implant and endplates. The device’s fenestrations allow for postoperative fusion assessment.

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Broad Clearance for Patient Optimization

VariLift provides proven clinical outcomes and fewer postoperative complications, allowing surgeons to approach any existing procedure conservatively.

  • Mini, Open Microscope
  • Unilateral TLIF, Bilateral PLIF
  • 1 or 2 Level Stand-Alone
  • Interbody with or without Supplemental Fixation
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VariLift®-LX Retrospective Study

Treatment of Symptomatic Lumbar Disc Degeneration with the VariLift-L Interbody Fusion System: Retrospective Review of 470 Cases

Published: 5/3/2016 | International Journal of Spine Surgery
Contributors:
Warren F. Neely, MD | Frank Fichtel, MD | Diana Cardenas del Monaco, PhD | Jon E. Block, PhD

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Flexible Treatment Option for Adjacent Segment Disease

VariLift® boasts significant clinical success and high fusion rates for the treatment of symptomatic ASD cases. Stand-Alone adjacent level treatment is an alternative approach to reduce VAS scores and clinical symptoms without the need for supplemental fixation.

A) Pre-operative MRI showing ASD, B) Post-operative lateral radiograph, C) Post-operative A/P radiograph with placement of the 2 standalone devices at L2-3 and L3-4 and continued presence of the pre-existing anterior/posterior fusion construct.

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VariLift®-LX is a Simple Option for Your Most Complicated Cases.

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