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Nuvasive Zero-P Implant
No active recall
Manufacturer: Nuvasive · FDA product code: OVE · Category: Intervertebral Fusion Device With Integrated Fixation, Cervical
Severity Snapshot
145 total reports2008-12 – 2025-02 date range4.2% physician / facility reported95.8% manufacturer reported30 SKU variants
Failure & Consequence Profiles
Top Failure Modes
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Top Patient Outcomes
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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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