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Nuvasive Catalyft PL Expandable Interbody
No active recall
Manufacturer: Nuvasive · FDA product code: MAX · Category: Intervertebral Fusion Device With Bone Graft, Lumbar
Severity Snapshot
304 total reports2022-01 – 2026-03 date range94.4% physician / facility reported5.6% manufacturer reported1 SKU variants
Failure & Consequence Profiles
Top Failure Modes
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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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