VariLift-LX -Stand-Alone Expandable Lumbar Interbody Fusion Device

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

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.

Stand-Alone Expandable Lumbar Interbody Fusion

• Device expands In Situ and provides lordotic correction
• Unique design allows for extensive use of graft material post implantation
• MIS Adjacent Segment Disease Solution
• Broad FDA Clearance allows device to be used with or without supplemental fixation

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.

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.

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.

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.

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.