510(k) Report

FDA applicant

Advanced Osseous Technologies

Mountain View, CA2 decisions1990–19910 recalls

FDA records 2 decisions for Advanced Osseous Technologies (Mountain View, CA) from 1990 to 1991: 2 510(k) clearances. All are in product code JDX (Instrument, Surgical, Sonic And…). 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 Advanced Osseous Technologies’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Advanced Osseous Technologies since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Advanced Osseous Technologies 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?

  • JDXInstrument, Surgical, Sonic And Accessory/Attachment2decisions

Who builds on its devices?

Later devices cite its devices 2 times; 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.

  • K900003System Ten Model 100 Surgical SystemAdvanced Osseous Technologies · 19902cite it

What has FDA decided for it lately?

  • K905451System Ten, Model 100 Surgery Syst/Orthopaedic UseAdvanced Osseous Technologies · 1991
  • K900003System Ten Model 100 Surgical SystemAdvanced Osseous Technologies · 1990

All 2 as Advanced Osseous Technologies →