FDA postpones panel meeting for VertiFlex's Superion spine device

The FDA postpones and relocates an advisory panel meeting that's slated for the Superion interspinous spacer made by VertiFlex.

The FDA postponed a meeting of 1 of its advisory panels that's slated to review the pre-market approval application for the Superion spine implant made by VertiFlex.

Food & Drug Administration (FDA), VertiFlex Inc.

News Well, Orthopedics, Pre-Market Approval (PMA), Regulatory/Compliance, Spinal

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