The Barricaid bone-anchored implant is the first device clinically proven to reduce the incidence of reherniation and reoperation in patients with large annular defects.

Barricaid is the only FDA PMA-approved technology indicated for reducing reherniation and reoperation after lumbar discectomy. The implant is anchored to healthy bone with a titanium …

Barricaid implantation follows your standard discectomy surgery. And Barricaid is built for the long haul. It’s designed to withstand 330 pounds per square inch of pressure—strong enough to …

Barricaid is clinically proven to reduce your risk of a second surgery and return of symptoms By closing the hole following your discectomy surgery, Barricaid greatly reduces the chance of …

Decades in the making, Barricaid is the only FDA-approved device designed to close large defects in the annulus. Barricaid allows you to preserve more of your patient’s disc while …

Barricaid Instructions for Use provides the FDA-approved instructions, indications/contraindications, warning, precautions, information for prescribers and summary …

Nov 12, 2024 · Intrinsic Therapeutics, Inc., the developer of the Barricaid, an FDA approved medical device proven to significantly reduce reherniations and reoperations following lumbar …

Oct 24, 2024 · Intrinsic Therapeutics, Inc., the developer of the Barricaid, an FDA approved medical device proven to significantly reduce reherniations and reoperations following lumbar …

Jul 11, 2022 · Barricaid was proven safe and effective in a rigorous study presented to the FDA. Based on this strong clinical data, the FDA approved the Barricaid device for implantation into …

To receive a list of surgeons in your area trained to diagnose and treat a lumbar disc herniation with Barricaid, please complete the form. Download Barricaid Introductory Guide for Patients »