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Neuroform Atlas 3
No active recall
FDA product code: NJE · Category: Intracranial Neurovascular Stent
Severity Snapshot
429 total reports2020-02 – 2026-03 date range86.2% physician / facility reported13.8% manufacturer reported11 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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