Back to DBS / Neuromodulation
Precision Spectra®
No active recall
FDA product code: LGW · Category: Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
Severity Snapshot
4,516 total reports2013-05 – 2017-03 date range0% physician / facility reported100% 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…