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Wingspan Stent
No active recall
FDA product code: NJE · Category: Intracranial Neurovascular Stent
Severity Snapshot
454 total reports2006-01 – 2018-04 date range0.9% physician / facility reported99.1% manufacturer reported4 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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