FDA 510(k)

Arthrex Mini Hip PushLock

K-Number: K201786 · 2020-07-30

Decision Date2020-07-30

Product CodeMAI

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

Arthrex Mini Hip PushLock is a medical device manufactured by Arthrex, Inc.. It received FDA 510(k) clearance on 2020-07-30 under approval number K201786. The device is classified under product code MAI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Arthrex Mini Hip PushLock?

Arthrex Mini Hip PushLock is a medical device that received FDA 510(k) clearance on 2020-07-30. It is manufactured by Arthrex, Inc.. The 510(k) number is K201786.

When was Arthrex Mini Hip PushLock approved by the FDA?

Arthrex Mini Hip PushLock received FDA 510(k) clearance on 2020-07-30, under approval number K201786.

What company makes Arthrex Mini Hip PushLock?

Arthrex Mini Hip PushLock is manufactured by Arthrex, Inc..

What is the FDA product code for Arthrex Mini Hip PushLock?

The FDA product code for Arthrex Mini Hip PushLock is MAI.

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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.