MODIFICATION TO COOK ZILVER BILIARY STENT— 510(k) K031821

Unknown

Cook, Inc.

FDA 510(k) clearance K031821 for MODIFICATION TO COOK ZILVER BILIARY STENT, Unknown on 2003-07-18. Applicant: Cook, Inc..

Clearance details

Applicant: Cook, Inc.
Product code: Code FGE
Advisory panel: Gastroenterology, Urology
Date received: 2003-06-13
Decision date: 2003-07-18
Decision: Unknown
Clearance type: Special
Location: Bloomington, IN, US

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Adverse events under product code FGE

product code FGE

Death: 52
Injury: 2,347
Malfunction: 9,798
Other: 1
Total: 12,198

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.