# Medtronic Neurological

- Location (FDA's records): Minneapolis, MN
- FDA decisions: 2 (2001–2003): 2 510(k) clearances
- Product codes: GZB (2)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Medtronic Vascular: 3 (https://510kreport.com/company/medtronic-vascular)
- Medtronic Neuromodulation: 1 (https://510kreport.com/company/medtronic-neuromodulation)

## Firms that cite its devices most
- Medtronic Vascular: 1 (https://510kreport.com/company/medtronic-vascular)

## Its most-cited devices
- K033016: Pisces Z Quad Lead Model, 3890, Pisces Z Quad Compact Lead Model, 3891, Pisces Z Quad Plus Lead Model, 3892 (2003), cited by 1

## Recent decisions
- K033016: Pisces Z Quad Lead Model, 3890, Pisces Z Quad Compact Lead Model, 3891, Pisces Z Quad Plus Lead Model, 3892 (Oct 30, 2003)
- K013063: Grip Lock Anchor, Model 411374 (Dec 11, 2001)

Source page: https://510kreport.com/company/medtronic-neurological