3D ANATOMICAL MESH— 510(k) K990930

Substantially Equivalent

Santerra Medical Technology, Inc.

FDA 510(k) clearance K990930 for 3D ANATOMICAL MESH, Substantially Equivalent on 1999-06-17. Applicant: Santerra Medical Technology, Inc..

Clearance details

Applicant: Santerra Medical Technology, Inc.
Product code: Code FTL
Advisory panel: General, Plastic Surgery
Date received: 1999-03-19
Decision date: 1999-06-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lake Elmo, MN, US

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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.