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Nuvasive Anchor C Diam 3
No active recall
Manufacturer: Nuvasive · FDA product code: OVE · Category: Intervertebral Fusion Device With Integrated Fixation, Cervical
Severity Snapshot
167 total reports2011-11 – 2026-03 date range4.8% physician / facility reported95.2% manufacturer reported15 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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