BEUDAMED
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    Filters Classification: Class Ii ×

    Barricaid Annual Closure Device (ACD) BAR-A8-8MM - Product Usage: The Barricaid¿ ACD is indicated for reducing the incidence of reherniation, and reoperation in skeletally mature patients with radiculopathy (with or without back pain) attributed to a posterior or posterolateral herniation, and confirmed by history, physical examination and imaging studies which demonstrate neural compression using MRI to treat a large annular defect (between 4-6 mm tall and between 6-10 mm wide) following a primary discectomy procedure (excision of herniated intervertebral disc) at a single level between L4 and S1.

    FDA Enforcement
    Class II ·Terminated·Intrinsic Therapeutics, Inc.·August 19, 2020

    Barricaid Annular Closure Impactor, REF: BAR-IMPACTOR, P/N: 400906-A

    FDA Enforcement
    Class II ·Ongoing·Intrinsic Therapeutics, Inc.·August 28, 2024