SUPERSTITCH VASCULAR SUTURING DEVICE, 6 FRENCH, MODELS 06-15-00X; MID-LENGTH 06-25-00X— 510(k) K020940

Substantially Equivalent

Sutura, Inc.

FDA 510(k) clearance K020940 for SUPERSTITCH VASCULAR SUTURING DEVICE, 6 FRENCH, MODELS 06-15-00X; MID-LENGTH 06-25-00X, Substantially Equivalent on 2002-04-17. Applicant: Sutura, Inc..

Clearance details

Applicant: Sutura, Inc.
Product code: Code GAW
Advisory panel: General, Plastic Surgery
Date received: 2002-03-22
Decision date: 2002-04-17
Decision: Substantially Equivalent
Clearance type: Special
Location: Fountain Valley, CA, US

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Adverse events under product code GAW

product code GAW

Death: 66
Injury: 1,616
Malfunction: 10,428
Total: 12,110

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.