510(k) Report

FDA applicant

Patrick Berdoz

Chester Springs, PA1 decision2000–20000 recalls

FDA records 1 decision for Patrick Berdoz (Chester Springs, PA) in 2000: 1 510(k) clearance. All are in product code HRS (Plate, Fixation, Bone). 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 Patrick Berdoz’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Patrick Berdoz since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Patrick Berdoz 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?

  • HRSPlate, Fixation, Bone1decision

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.

  • K002486Precimed Trauma SystemPatrick Berdoz · 20001cites it

What has FDA decided for it lately?

  • K002486Precimed Trauma SystemPatrick Berdoz · 2000

The one decision as Patrick Berdoz →

Other applicant names beginning “Patrick”

FDA records each applicant name separately; these may or may not be the same firm.

Patrick C. Jacobssen 1Patrick D. Mcgrath Ph.D 1Patrick J. O'Regan 1