Back to Nuvasive
Nuvasive Anteralign Spinal System With Titan Nanolock
No active recall
Manufacturer: Nuvasive · FDA product code: MAX · Category: Intervertebral Fusion Device With Bone Graft, Lumbar
Severity Snapshot
69 total reports2022-11 – 2026-03 date range95.7% physician / facility reported4.3% manufacturer reported1 SKU variants
Reporting Trend
Annual Reporting Volume
Click any bar to view those reports ↓
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.
Loading reports…