AMT T-FASTENER ANCHOR KIT— 510(k) K120587

Unknown

Applied Medical Technology, Inc.

FDA 510(k) clearance K120587 for AMT T-FASTENER ANCHOR KIT, Unknown on 2012-05-25. Applicant: Applied Medical Technology, Inc..

Clearance details

Applicant: Applied Medical Technology, Inc.
Product code: Code KGC
Advisory panel: Gastroenterology, Urology
Date received: 2012-02-27
Decision date: 2012-05-25
Decision: Unknown
Clearance type: Traditional
Location: Brecksville, OH, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code KGC

product code KGC

Death: 7
Total: 7

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.