FDA 510(k)

Arthrex PushLock

K-Number: K173240 · 2018-01-16

Decision Date2018-01-16

Product CodeMAI

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

Arthrex PushLock is a medical device manufactured by Arthrex, Inc.. It received FDA 510(k) clearance on 2018-01-16 under approval number K173240. 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 PushLock?

Arthrex PushLock is a medical device that received FDA 510(k) clearance on 2018-01-16. It is manufactured by Arthrex, Inc.. The 510(k) number is K173240.

When was Arthrex PushLock approved by the FDA?

Arthrex PushLock received FDA 510(k) clearance on 2018-01-16, under approval number K173240.

What company makes Arthrex PushLock?

Arthrex PushLock is manufactured by Arthrex, Inc..

What is the FDA product code for Arthrex PushLock?

The FDA product code for Arthrex 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.