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Dorsal Root Ganglion Stimulator For Pain Relief
FDA product code PMP · Class 3 · Unknown
45
Registered devices
19,735
Adverse events
2
Recalls
0
510(k) clearances
Devices with this code
Axium™ — SPINAL MODULATION, INC.Axium™ — SPINAL MODULATION, INC.NA — ADVANCED NEUROMODULATION SYSTEMS, INC.Axium™ — SPINAL MODULATION, INC.Axium™ — ST. JUDE MEDICAL, INC.NA — ADVANCED NEUROMODULATION SYSTEMS, INC.Axium™ — SPINAL MODULATION, INC.NA — ST. JUDE MEDICAL, INC.Axium™ — SPINAL MODULATION, INC.NA — ST. JUDE MEDICAL, INC.SlimTip™ — ADVANCED NEUROMODULATION SYSTEMS, INC.Axium™ — SPINAL MODULATION, INC.NA — ST. JUDE MEDICAL, INC.Axium™ — ST. JUDE MEDICAL, INC.Axium™ — ST. JUDE MEDICAL, INC.NA — ST. JUDE MEDICAL, INC.NeuroSphere™ — ADVANCED NEUROMODULATION SYSTEMS, INC.Axium™ — ST. JUDE MEDICAL, INC.NA — ST. JUDE MEDICAL, INC.Axium™ — ST. JUDE MEDICAL, INC.Axium™ — SPINAL MODULATION, INC.Proclaim™ — ADVANCED NEUROMODULATION SYSTEMS, INC.Axium™ — ST. JUDE MEDICAL, INC.SJM™ — ST. JUDE MEDICAL, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-05-16 | Abbott Medical | The duration between the implantable pulse generator reaching the elective replacement indicator threshold and end of service may be shorter than indicated in |
| 2018-03-09 | St. Jude Medical, Inc. | The firm received complaints of error messages that occurred during routine impedance checks on Proclaim DRG IPGs, model 3664. Some complaints were also associ |
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