510(k) Report

FDA applicant

Medtronic-Synectics

Stockholm, SE1 decision1997–19970 recalls

FDA records 1 decision for Medtronic-Synectics (Stockholm, SE) in 1997: 1 510(k) clearance. All are in product code FFX (System, Gastrointestinal Motility (Electrical)). Its devices cite 1 predicate, 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, gastroenterology and urology panel, where it files most

How often FDA has decided Medtronic-Synectics’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medtronic-Synectics since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Medtronic-Synectics 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?

  • FFXSystem, Gastrointestinal Motility (Electrical)1decision

Whose devices does it build on?

Its devices cite 1 predicate; 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.

  • K972439Anorectal Manometry Analysis ModuleMedtronic-Synectics · 19971cites it

What has FDA decided for it lately?

  • K972439Anorectal Manometry Analysis ModuleMedtronic-Synectics · 1997

The one decision as Medtronic-Synectics →