Lumbar Spinal Stenosis
What is Lumbar Spinal Stenosis (LSS)?

Lumbar Spinal Stenosis is caused by changes in the shape and size of the spinal canal as we age. This natural degenerative process can cause anatomical changes at any time, but is most common in people over 50 years and may continue to progress with age.

Talk with your Georgia Pain and Wellness Center doctor about Superion if you have any of the following symptoms:

Leg, buttock, and groin pain
Numbness, weakness, cramping, or stiffness in the legs, or buttocks
Difficulty walking or standing but experience relief in the seated or flexed position

How does Superion treat LSS?
Superion is a completely new, minimally invasive approach to treating lumbar stenosis that fills a gap in the continuum between conservative care and invasive surgery. Designed with patient safety and comfort in mind, Superion is implanted through a small tube the size of a dime to reduce tissue damage and blood loss. It’s a simple outpatient procedure with a rapid recovery time and no destabilization of the spine.

Indirect Decompression

The Superion implant acts as an indirect decompression device. Its anatomic design provides optimal fit and preserves a patient’s anatomy and ability to maintain motion. Superion acts as an extension blocker, relieving pressure on the affected nerves in the manner that one would achieve relief in a seated or flexed position. Available in multiple sizes to accommodate varying patient anatomy, Superion ensures controlled movement and minimizes post-procedure complications. Superion was developed to provide patients with a safe and effective alternative when conservative treatment has failed and laminectomy is too aggressive.

FDA approved, Superion is clinically shown to be effective for up to 48 months. Certain risks are associated with the use of Superion. Consult your doctor for more information regarding these risks.

Superion acts as an extension blocker, relieving pressure on the affected nerves.

To make an appointment to determine if you are a candidate for this FDA approved minimally invasive procedure, go to: or call (770)962-3642.