Intrinsic Therapeutics, Inc.
FDA 510(k) medical device clearance, cleared in 2020, with 2 FDA device recalls on record.
Top product codes for Intrinsic Therapeutics, Inc.
FDA recalls by Intrinsic Therapeutics, Inc.
- Z-2688-2024 — Barricaid Annular Closure Impactor, REF: BAR-IMPACTOR, P/N: 400906-A
- Z-2798-2020 — 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.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Intrinsic Therapeutics, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.