Back to Spinal Implants
M6-C
No active recall
FDA product code: MJO · Category: Prosthesis, Intervertebral Disc
Severity Snapshot
440 total reports2017-11 – 2026-03 date range46.9% physician / facility reported53.1% 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…