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Manufacturer: Nuvasive · FDA product code: MAX · Category: Intervertebral Fusion Device With Bone Graft, Lumbar
Severity Snapshot
78 total reports2011-03 – 2022-04 date range0% physician / facility reported100% manufacturer reported33 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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