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These include several devices with a European Conformity (CE) mark or limited US Food and Drug Administration (FDA) approval that are based on surgical placement of custom-tailored sutures or polymeric meshes over the annular defect site, and fixed with anchors typically attached to bone (e.g., XClose® Surgical Repair, Inclose™ Surgical Mesh, Barricaid™) (Figure 2)

This sleek