MESO WOUND MATRIX— 510(k) K112888

Substantially Equivalent

Kensey Nash Corporation

FDA 510(k) clearance K112888 for MESO WOUND MATRIX, Substantially Equivalent on 2012-02-10. Applicant: Kensey Nash Corporation.

Clearance details

Applicant: Kensey Nash Corporation
Product code: Code KGN
Advisory panel: Unknown
Date received: 2011-09-30
Decision date: 2012-02-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Exton, PA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code KGN

product code KGN

Other: 2
Total: 2

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.