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FDA 510(k)

MyKnee R Pin Positioners

K-Number: K220705 · 2022-05-04

Decision Date2022-05-04
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MyKnee R Pin Positioners is a medical device manufactured by Medacta International S.A.. It received FDA 510(k) clearance on 2022-05-04 under approval number K220705. 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 MyKnee R Pin Positioners?

MyKnee R Pin Positioners is a medical device that received FDA 510(k) clearance on 2022-05-04. It is manufactured by Medacta International S.A.. The 510(k) number is K220705.

When was MyKnee R Pin Positioners approved by the FDA?

MyKnee R Pin Positioners received FDA 510(k) clearance on 2022-05-04, under approval number K220705.

What company makes MyKnee R Pin Positioners?

MyKnee R Pin Positioners is manufactured by Medacta International S.A..

What is the FDA product code for MyKnee R Pin Positioners?

The FDA product code for MyKnee R Pin Positioners is JWH.

Other Devices by Medacta International S.A.

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Related Devices (Code: JWH)

Official Source

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