K951675

Substantially Equivalent

GORE-TEX MYCROMESH BIOMATERIAL

Applicant: W. L. Gore & Associates, Inc.
Product code: FTL
Advisory panel: General, Plastic Surgery
Date received: 1995-04-11
Decision date: 1995-10-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Elkton, MD, US

Adverse events under product code FTL

product code FTL

Death: 317
Injury: 66,072
Malfunction: 1,273
Other: 3
Total: 67,665

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.