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Nuvasive Oasys Blocker
No active recall
Manufacturer: Nuvasive · FDA product code: NKG · Category: Posterior Cervical Screw System
Severity Snapshot
106 total reports2005-02 – 2024-01 date range8.5% physician / facility reported91.5% 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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