Skip Navigation
Skip Main Content

FDA-APPROVED BARRICAID | DISC HERNIATION TREATMENT

Barricaid®

Living with a herniated disc can be frustrating, especially if symptoms return after surgery. After a microdiscectomy , a procedure that removes damaged disc material, the disc can still reherniate, particularly if there's a large opening or weak spot in the outer part of the disc. The Barricaid device was designed to resolve this issue.

Barricaid is the only FDA-approved annular closure device designed to repair large defects in the outer layer of a herniated disc. By sealing the weakened area, it reduces the risk of another herniation and provides patients with a stronger, longer-lasting outcome after surgery.

At Surgical Spine Associates, our experienced team uses Barricaid as part of a minimally invasive microdiscectomy procedure. We specialize in precise, cutting-edge treatments that give patients the best possible chance of lasting relief.

If you’re considering surgery for a disc herniation, we encourage you to learn more about whether the Barricaid spine implant may be right for you. Request an appointment today to explore your options.

Appointments

Senior female suffering from back pain

HOW THE BARRICAID ANNULAR CLOSURE DEVICE WORKS

Reducing the Risk of Reherniation

When a disc herniates, it creates a defect in the disc’s outer layer, known as the annulus. During a microdiscectomy, the herniated material is removed, but that opening in the annulus remains. If the defect is large enough, the likelihood of a second herniation rises sharply. This is where the Barricaid device can help.

After the disc material is removed, the surgeon carefully measures the size of the defect. If it meets the criteria, the Barricaid implant is anchored to the neighboring vertebra, and a flexible mesh flap covers the opening. This reinforcement strengthens the disc wall and reduces the risk of fragments escaping in the future. By directly addressing the weak spot, Barricaid provides patients with added security and protection that traditional microdiscectomy alone cannot.

At Surgical Spine Associates, our surgeons incorporate Barricaid into treatment when it is the safest and most effective choice. With decades of surgical experience and a dedication to minimally invasive spine care, we deliver advanced solutions like the Barricaid device in a way that prioritizes precision, safety, and long-term results.

Frequently Asked Questions

What makes the Barricaid device different from traditional disc surgery?

Standard microdiscectomy surgery removes damaged disc material but does not repair the weakened annulus (the disc’s outer ring). The Barricaid device addresses this gap by sealing the defect, creating a barrier that helps prevent another herniation. This significantly lowers the risk of needing a second surgery.

Am I a candidate for the Barricaid annular closure device?

Patients who qualify typically have a large annular defect discovered during microdiscectomy surgery. Your surgeon will measure the defect after removing the herniated portion of the disc. If it meets the criteria, the Barricaid device may be recommended as part of your treatment plan.

Is the Barricaid device safe?

Yes! Barricaid is the only FDA-approved annular closure device and has been studied in thousands of patients worldwide. Like any procedure, there are risks, but Barricaid has been shown to significantly reduce reherniation rates compared to surgery alone. Your surgeon will discuss the potential benefits and risks with you during your consultation.

How do I schedule a consultation for Barricaid?

Scheduling is simple. You can call us at (412) 275-0227 or use our online booking system to request an appointment. Our team will confirm your insurance coverage and guide you through every step. We look forward to helping you find relief!

PREVENT REHERNIATION & MOVE FORWARD WITH CONFIDENCE

Precision Care for a Stronger Tomorrow

Appointments