Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

360CAS Knee

K-Number: K242009 · 2024-08-08

ApplicantKico Knee Innovation Company Pty, Ltd.
Decision Date2024-08-08
Product CodeOLO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

360CAS Knee is a medical device manufactured by Kico Knee Innovation Company Pty, Ltd.. It received FDA 510(k) clearance on 2024-08-08 under approval number K242009. The device is classified under product code OLO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 360CAS Knee?

360CAS Knee is a medical device that received FDA 510(k) clearance on 2024-08-08. It is manufactured by Kico Knee Innovation Company Pty, Ltd.. The 510(k) number is K242009.

When was 360CAS Knee approved by the FDA?

360CAS Knee received FDA 510(k) clearance on 2024-08-08, under approval number K242009.

What company makes 360CAS Knee?

360CAS Knee is manufactured by Kico Knee Innovation Company Pty, Ltd..

What is the FDA product code for 360CAS Knee?

The FDA product code for 360CAS Knee is OLO.

Other Devices by Kico Knee Innovation Company Pty, Ltd.

K243950ARVIS® Shoulder

Related Devices (Code: OLO)

K162375Envision 3D: Image Guidance System7D Surgical, Inc. K162341Stryker OrthoMap Precision Knee systemStryker Leibinger GmbH & Co KG K162195TSolution One Cup1 Surgical SystemTHINK Surgical, Inc. K160385Precision ScrewCryptych Pty, Ltd. K153700Aesculap(R) Implant Systems (AIS) S4 Navigation InstrumentsAesculap Implant Systems, LLC K153240Styrker OrthoMap Express Knee SystemStryker Corporate

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑