# St. Jude Medical Neuromodulation

- Location (FDA's records): Plano, TX
- FDA decisions: 2 (2011–2013): 2 510(k) clearances
- Product codes: GZB (2)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Advanced Neuromodulation Systems: 2 (https://510kreport.com/company/advanced-neuromodulation-systems)

## Recent decisions
- K123299: MTS System, Wide-Space Quattrode Percutaneous Leads (Jan 18, 2013)
- K112214: Octrodex (TM), Quattrodex (TM), Introdex (TM), Epidural Needle, Stylets (Nov 17, 2011)

Source page: https://510kreport.com/company/st-jude-medical-neuromodulation