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FDA 510(k)

Unity Total Knee System

K-Number: K173884 · 2018-01-17

Decision Date2018-01-17
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Unity Total Knee System is a medical device manufactured by Corin U.S.A. Limited. It received FDA 510(k) clearance on 2018-01-17 under approval number K173884. 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 Unity Total Knee System?

Unity Total Knee System is a medical device that received FDA 510(k) clearance on 2018-01-17. It is manufactured by Corin U.S.A. Limited. The 510(k) number is K173884.

When was Unity Total Knee System approved by the FDA?

Unity Total Knee System received FDA 510(k) clearance on 2018-01-17, under approval number K173884.

What company makes Unity Total Knee System?

Unity Total Knee System is manufactured by Corin U.S.A. Limited.

What is the FDA product code for Unity Total Knee System?

The FDA product code for Unity Total Knee System is JWH.

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Official Source

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