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Barricaid Annular Closure Device
Barricaid Recurrent Disc Herniation Solution
Barricaid's key value proposition is providing the only FDA-approved, clinically proven implant that significantly reduces reherniation and reoperation rates by closing large annular defects after discectomy. This leads to improved, durable outcomes and enhanced quality of life for patients, offering a 'superior intraoperative choice' for surgeons.
Barricaid is positioned as the leading and only FDA-approved bone-anchored implant for preventing reherniation after lumbar discectomy, specifically for patients with large annular defects. It offers a clinically proven solution for superior, long-term patient outcomes.
Globus Medical
Medtronic
NuVasive (part of Globus Medical)
Customer sentiment is likely positive, especially among surgeons seeking evidence-based solutions for better patient outcomes and patients desiring a durable fix to avoid reoperation and improve quality of life. The emphasis on clinical evidence (Level I RCT) and FDA approval instills confidence.
To strengthen brand positioning, Barricaid should highlight its unique, patented technology and superior long-term outcomes to further differentiate itself from traditional approaches and potential competitors.
The Barricaid Annular Closure Device is an FDA-approved medical device specifically designed to close large defects in the annulus, the outer fibrous ring of the intervertebral disc. Its primary function is to prevent reherniation after discectomy surgery, thereby reducing the need for repeat surgeries and improving long-term patient outcomes. A key feature of Barricaid is its ability to preserve more of the patient's native disc tissue, which is crucial for maintaining spinal biomechanics and function. This device is intended for use in patients undergoing lumbar discectomy for single-level, primary disc herniation.
Herniated disc surgery patients benefit from Barricaid, offering a breakthrough solution to lower the risk of reherniation and reoperation in herniated disc ...
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View sourceOct 24, 2024 ... Intrinsic Therapeutics, Inc., the developer of the Barricaid, an FDA approved medical device proven to significantly reduce reherniations ...
View sourceThis brochure will provide you with information about the Barricaid® Annular. Closure Device (ACD), also referred to as “Barricaid,” a new treatment intended.
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