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Nuvasive T-Pal Spacer Applicator Inner Shaft
No active recall
Manufacturer: Nuvasive · FDA product code: MAX · Category: Intervertebral Fusion Device With Bone Graft, Lumbar
Severity Snapshot
190 total reports2015-12 – 2024-10 date range5.3% physician / facility reported94.7% manufacturer reported3 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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