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Superion Indirect Decompression
No active recall
FDA product code: NQO · Category: Prosthesis, Spinous Process Spacer/Plate
Severity Snapshot
1,787 total reports2017-09 – 2026-03 date range73.9% physician / facility reported26.1% manufacturer reported2 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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