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FDA 510(k)

World Knee System

K-Number: K180750 · 2018-04-20

ApplicantSignature Orthopaedics Pty, Ltd.
Decision Date2018-04-20
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

World Knee System is a medical device manufactured by Signature Orthopaedics Pty, Ltd.. It received FDA 510(k) clearance on 2018-04-20 under approval number K180750. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the World Knee System?

World Knee System is a medical device that received FDA 510(k) clearance on 2018-04-20. It is manufactured by Signature Orthopaedics Pty, Ltd.. The 510(k) number is K180750.

When was World Knee System approved by the FDA?

World Knee System received FDA 510(k) clearance on 2018-04-20, under approval number K180750.

What company makes World Knee System?

World Knee System is manufactured by Signature Orthopaedics Pty, Ltd..

What is the FDA product code for World Knee System?

The FDA product code for World Knee System is JWH.

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Related PubMed Literature

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Other Devices by Signature Orthopaedics Pty, Ltd.

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Related Devices (Code: JWH)

K160515PS2 Knee SystemConsensus Orthopedics, Inc. K160771Destiknee Total Knee SystemMeril Healthcare Private Limited K160157LOSPA Modular Knee SystemCorentec Co., Ltd. K162273Materialise TKA Guide SystemMaterialise NV K162422Klassic Knee SystemTotal Joint Orthopedics, Inc. K161945EXPRT Revision Knee Femoral Augment(5mm), EXPRT Revision Knee Stem Extension (40mm)Encore Medical L.P.

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.

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