FDA applicant
Advanced Neuromodulation System,Inc
FDA records 1 decision for Advanced Neuromodulation System,Inc (Plano, TX) in 2002: 1 510(k) clearance. All are in product code GZB (Stimulator, Spinal-Cord, Implanted (Pain Relief)). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Advanced Neuromodulation System,Inc’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Advanced Neuromodulation System,Inc since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Advanced Neuromodulation System,Inc’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report