FDA applicant

Vertebral Technologies, Inc.

Minneapolis, MN7 decisions2008–20130 recalls

FDA records 7 decisions for Vertebral Technologies, Inc. (Minneapolis, MN) from 2008 to 2013: 7 510(k) clearances. All are in product code MAX (Intervertebral Fusion Device With Bone Graft…). Its devices cite 10 predicates, 7 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, orthopedic panel, where it files most

How often FDA has decided Vertebral Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2013

2008high 2 (2009) · low 0 (2012)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2008.

FIG. 1 — Vertebral Technologies, Inc. by year, 2008–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Vertebral Technologies, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Vertebral Technologies, Inc.

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?