# Medtronic Inc.,Neurological Division.

- Location (FDA's records): Miinneapolis, MN
- FDA decisions: 1 (2005–2005): 1 510(k) clearance
- Product codes: GZB (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K051773: Model 3873 1* 8 and Model 3874 1* 8 Compact Test Stimulation Leads (Jul 28, 2005)

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