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FDA 510(k)

Arthrex PushLock Tenodesis Anchor

K-Number: K181513 · 2018-08-30

ApplicantArthrex, Inc.
Decision Date2018-08-30
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Arthrex PushLock Tenodesis Anchor is a medical device manufactured by Arthrex, Inc.. It received FDA 510(k) clearance on 2018-08-30 under approval number K181513. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Arthrex PushLock Tenodesis Anchor?

Arthrex PushLock Tenodesis Anchor is a medical device that received FDA 510(k) clearance on 2018-08-30. It is manufactured by Arthrex, Inc.. The 510(k) number is K181513.

When was Arthrex PushLock Tenodesis Anchor approved by the FDA?

Arthrex PushLock Tenodesis Anchor received FDA 510(k) clearance on 2018-08-30, under approval number K181513.

What company makes Arthrex PushLock Tenodesis Anchor?

Arthrex PushLock Tenodesis Anchor is manufactured by Arthrex, Inc..

What is the FDA product code for Arthrex PushLock Tenodesis Anchor?

The FDA product code for Arthrex PushLock Tenodesis Anchor is MBI.

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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.

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