Kerecis Parvus (50207)— 510(k) K241080

Substantially Equivalent

Kerecis Limited

FDA 510(k) clearance K241080 for Kerecis Parvus (50207), Substantially Equivalent on 2024-08-21. Applicant: Kerecis Limited.

Clearance details

Applicant: Kerecis Limited
Product code: Code KGN
Advisory panel: Unknown
Date received: 2024-04-19
Decision date: 2024-08-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Isafjordur, IS

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.