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Bryan Cervical Disc
No active recall
FDA product code: MJO · Category: Prosthesis, Intervertebral Disc
Severity Snapshot
272 total reports2009-08 – 2023-08 date range0.4% physician / facility reported99.6% manufacturer reported2 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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