FDA applicant

V. Mueller Neuro/Spine

San Carlos, CA8 decisions1994–20000 recalls

FDA records 8 decisions for V. Mueller Neuro/Spine (San Carlos, CA) from 1994 to 2000: 8 510(k) clearances. Most are in product codes HCH (Clip, Aneurysm) and HBA (Neurosurgical Paddie). Its devices cite 2 predicates, 1 of them its own earlier devices. 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 V. Mueller Neuro/Spine’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for V. Mueller Neuro/Spine since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — V. Mueller Neuro/Spine by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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V. Mueller Neuro/Spine

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?