510(k) Report

FDA applicant

Medtronic Spinal and Biologics Div

Memphis, TN1 decision2006–20060 recalls

FDA records 1 decision for Medtronic Spinal and Biologics Div (Memphis, TN) in 2006: 1 510(k) clearance. All are in product code MQP (Spinal Vertebral Body Replacement Device). Its devices cite 2 predicates, 0 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 Medtronic Spinal and Biologics Div’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medtronic Spinal and Biologics Div since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • MQPSpinal Vertebral Body Replacement Device1decision

Whose devices does it build on?

Its devices cite 2 predicates; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K062133Modification to Verte-Stack Spinal SystemMedtronic Spinal and Biologics Div · 20061cites it

What has FDA decided for it lately?

  • K062133Modification to Verte-Stack Spinal SystemMedtronic Spinal and Biologics Div · 2006

The one decision as Medtronic Spinal and Biologics Div →