Barricaid
Commercial- Indications
- Lumbar disc herniation, Recurrent disc herniation
Company intelligence / Profile preview
Barricaid®, the company’s proprietary bone-anchored annular closure device, is commercially available and has been implanted in over 12,000 patients. Multiple clinical studies—including two randomized controlled trials and six single-arm trials—demonstrate that Barricaid reduces reherniation and reoperation rates by up to 81% compared to discectomy alone. Five-year follow-up data published in JAMA confirm its superiority over standard care for high-risk patients with large annular defects.
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