# Advanced Neuromodulation Systems

- Location (FDA's records): Plano, TX
- FDA decisions: 25 (1999–2009): 25 510(k) clearances
- Product codes: GZB (24), GZF (1)
- Predicates its devices cite: 10 (1 its own); citations of its devices by later devices: 10 (1 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Neuromed, Inc.: 6 (https://510kreport.com/company/neuromed)
- Medtronic Vascular: 3 (https://510kreport.com/company/medtronic-vascular)

## Firms that cite its devices most
- Stimwave Technologies Incorporated: 2 (https://510kreport.com/company/stimwave-technologies)
- St Jude Medical: 2 (https://510kreport.com/company/st-jude-medical)
- St. Jude Medical Neuromodulation: 2 (https://510kreport.com/company/st-jude-medical-neuromodulation)
- Stimq, LLC: 1 (https://510kreport.com/company/stimq)
- Bioventus, LLC: 1 (https://510kreport.com/company/bioventus)
- Anulex Technologies, Inc.: 1 (https://510kreport.com/company/anulex-technologies)

## Its most-cited devices
- K000852: Renew Neurostimulation System (2001), cited by 4
- K092371: Swift-Lock Anchor, Model 1192 (2009), cited by 2
- K991784: Renew Lead Extension (1999), cited by 1
- K072462: Wide Spaced Quattrode Leads (2007), cited by 1
- K070847: Trial Cable, 3009 (2007), cited by 1
- K033757: MTS Multiprogram Trial Stimulator System (2004), cited by 1

## Recent decisions
- K092371: Swift-Lock Anchor, Model 1192 (Dec 23, 2009)
- K090907: Penta Lead Kits, Models: 3227-3234 (Jun 2, 2009)
- K081208: Cinch Anchor, Model 1194 (Jul 18, 2008)
- K072462: Wide Spaced Quattrode Leads (Oct 11, 2007)
- K070847: Trial Cable, 3009 (Apr 11, 2007)
- K063080: Tripole 8C and 16C and Exclaim 8 Lamitrode Series Leads (Dec 12, 2006)
- K053250: Ans 90 CM and 110 CM (3100 and 3200 Series) Lead Kit (Dec 15, 2005)
- K052374: Rapid Progeammer 3.0 (Nov 22, 2005)

Source page: https://510kreport.com/company/advanced-neuromodulation-systems