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No active recall
FDA product code: NQO · Category: Prosthesis, Spinous Process Spacer/Plate
Severity Snapshot
396 total reports2007-05 – 2012-09 date range1% physician / facility reported99% manufacturer reported1 SKU variants
Reporting Trend
Annual Reporting Volume
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Note: the 2018 Voluntary Malfunction Summary Reporting expansion means volume increases may reflect surveillance changes, not increased device risk.
Reported Events
Submitted to FDA MAUDE by physicians, hospitals, manufacturers, and patients.
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