FDA applicant

Medtronic Inc.,Neurological Division.

Miinneapolis, MN1 decision2005–20050 recalls

FDA records 1 decision for Medtronic Inc.,Neurological Division. (Miinneapolis, MN) in 2005: 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, last Nov 3, 2026

FIG. A — Illustration, neurology panel, where it files most

How often FDA has decided Medtronic Inc.,Neurological Division.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medtronic Inc.,Neurological Division. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Medtronic Inc.,Neurological Division. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Medtronic Inc.,Neurological Division.

Which product codes does it file in?

What has FDA decided for it lately?