360CAS Knee— 510(k) K242009

Name: FDA 510(k) clearance K242009
Creator: U.S. Food and Drug Administration
Published: 2024-08-08

Substantially Equivalent

Kico Knee Innovation Company Pty, Ltd.

FDA 510(k) clearance K242009 for 360CAS Knee, Substantially Equivalent on 2024-08-08. Applicant: Kico Knee Innovation Company Pty, Ltd.. Device class: 2.

Clearance details

Applicant: Kico Knee Innovation Company Pty, Ltd.
Product code: Code OLO
Device class: Class 2
Regulation: 21 CFR 882.4560
Advisory panel: Neurology
Date received: 2024-07-10
Decision date: 2024-08-08
Decision: Substantially Equivalent
Clearance type: Special
Location: Frenchs Forest, AU

Download summary PDF View on FDA.gov ↗

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Adverse events under product code OLO

product code OLO

Death: 11
Injury: 2,799
Malfunction: 11,105
Other: 1
Total: 13,916

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.