The Vertiflex™ Procedure†:
Make space for life
When simple activities such as walking or standing become a burden, you may find relief from leg and back pain with the Vertiflex Procedure.
What is lumbar spinal stenosis (LSS)?
Leg and back pain may be the result of a condition called lumbar spinal stenosis. LSS leads to the narrowing of the space in the lower (or lumbar) spine where nerves pass through. The narrowing of the space causes constriction on the nerves, which may result in pain and discomfort down the back and into the legs.
Pain is usually worsened when standing or walking, and leaning forward or sitting down provides relief. For most people, LSS develops gradually over time and is most common in adults over the age of 60.
Symptoms of LSS often include:
- Pain while walking or standing
- Weakness in legs
- Loss of balance
- Decreased physical endurance
- Numbness or tingling in the legs, buttocks, or back
- Aching, dull back pain spreading to legs
- Tendency to sit or lean over to relieve pain
Learn about LSS and the Vertiflex Procedure
Watch how the Vertiflex Procedure can relieve leg and back pain associated with LSS.
How does the Vertiflex Procedure work?
The Vertiflex Procedure is a safe, minimally invasive treatment that has been clinically proven to provide effective long-term relief from the pain associated with LSS.
- FDA approved
- Same-day procedure
- Quick recovery time
- Covered by Medicare and Medicaid
A small spacer is placed inside the spine without removal of any nearby bone or tissue.
Once inserted, the spacer’s arms open around the spinous processes (the bumps you can feel in your spine) to help make proper space for the affected nerves.
The spacer preserves the space in the spine, which keeps pressure off the nerves that cause leg and back pain.
How does the Vertiflex Procedure fit my pain?
The Vertiflex Procedure is intended to provide the same relief you experience when leaning forward or sitting down. It fits your pain by reducing or eliminating the pressure on the nerves caused by LSS. The spacer is also available in several different sizes to fit your anatomy.
Is it safe?
The Vertiflex Procedure was developed with patient safety and comfort in mind.
Its minimally invasive approach is preferred among many doctors across the United States.
General anesthesia is not required and there is minimal recovery time, getting you home the same day.
The spacer is designed to support your existing anatomy and does not require removal of bone or tissue, making it a safe option for LSS treatment.
Is it effective?
The Vertiflex Procedure was the subject of an extremely thorough FDA clinical trial for LSS. Results from the trial proved the effectiveness of the procedure, with significant improvement in pain relief.
The procedure can be completed in an outpatient setting and most patients can return home within the same day.
The minimally invasive Vertiflex Procedure is FDA approved and backed by a long-term clinical study.
Over 20,000 patients have received pain relief from the Vertiflex Procedure since FDA approval.
In the clinical study, most patients on opioids stopped using them after the Vertiflex Procedure.1,*
Nine out of ten patients in the clinical study were satisfied with their pain relief and increase in physical activity.2,‡
Life after the Vertiflex Procedure
The Vertiflex Procedure has helped thousands of people return to enjoying their day-to-day life again.
Wondering if the Vertiflex Procedure may be right for you?
Take this quick quiz and find out. ⟶
†Superion™ Indirect Decompression System.
*Decrease in the proportion of patients using opioids compared to baseline at five years.
References: 1. Nunley PD, Deer TR, Benyamin RM, Staats PS, Block JE. Interspinous process decompression is associated with a reduction in opioid analgesia in patients with lumbar spinal stenosis. Pain Res. 2018;11:2943-2948. 2. Nunley PD, Patel VV, Orndorff DG, Lavelle WF, Block JE, Geisler FH. Five-year durability of stand-alone interspinous process decompression for lumbar spinal stenosis. Clin Interv Aging. 2017;12:1409-1417. N=88.
Results from clinical studies are not predictive of results in other studies. Results in other studies may vary.