ZIMMER A.T.S. 3000 AUTOMATIC TOURNIQUET SYSTEM— 510(k) K050411

Substantially Equivalent

Zimmer, Inc.

FDA 510(k) clearance K050411 for ZIMMER A.T.S. 3000 AUTOMATIC TOURNIQUET SYSTEM, Substantially Equivalent on 2005-09-02. Applicant: Zimmer, Inc..

Clearance details

Applicant: Zimmer, Inc.
Product code: Code KCY
Advisory panel: General, Plastic Surgery
Date received: 2005-02-17
Decision date: 2005-09-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dover, OH, US

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Adverse events under product code KCY

product code KCY

Malfunction: 868
Total: 868

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.