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FDA 510(k)

A3 Total Knee System

K-Number: K180493 · 2018-06-22

Decision Date2018-06-22
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

A3 Total Knee System is the device name listed in this FDA 510(k) record. The listed applicant is Beijing AK Medical Co., Ltd.. It received FDA 510(k) clearance on 2018-06-22 under 510(k) number K180493. 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 A3 Total Knee System?

A3 Total Knee System is a medical device that received FDA 510(k) clearance on 2018-06-22. The listed applicant is Beijing AK Medical Co., Ltd.. The 510(k) number is K180493.

When did A3 Total Knee System receive FDA 510(k) clearance?

A3 Total Knee System received FDA 510(k) clearance on 2018-06-22, under 510(k) number K180493.

Who is the listed applicant for A3 Total Knee System?

The FDA 510(k) record lists Beijing AK Medical Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for A3 Total Knee System?

The FDA product code for A3 Total Knee System is JWH.

Related Devices (Code: JWH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.