ologen Collagen Matrix— 510(k) K173223

Substantially Equivalent

Aeon Astron Europe B.V.

FDA 510(k) clearance K173223 for ologen Collagen Matrix, Substantially Equivalent on 2018-03-02. Applicant: Aeon Astron Europe B.V..

Clearance details

Applicant: Aeon Astron Europe B.V.
Product code: Code KGN
Advisory panel: Unknown
Date received: 2017-10-03
Decision date: 2018-03-02
Decision: Substantially Equivalent
Clearance type: Special
Location: Leiden, NL

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.