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Nuvasive Crescent Spinal
No active recall
Manufacturer: Nuvasive · FDA product code: MAX · Category: Intervertebral Fusion Device With Bone Graft, Lumbar
Severity Snapshot
300 total reports2009-04 – 2025-11 date range2% physician / facility reported98% manufacturer reported1 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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