FDA 510(k)

Arthrex NanoSuture Anchor

K-Number: K180118 · 2018-02-12

Decision Date2018-02-12

Product CodeMBI

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

Arthrex NanoSuture Anchor is a medical device manufactured by Arthrex, Inc.. It received FDA 510(k) clearance on 2018-02-12 under approval number K180118. 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 NanoSuture Anchor?

Arthrex NanoSuture Anchor is a medical device that received FDA 510(k) clearance on 2018-02-12. It is manufactured by Arthrex, Inc.. The 510(k) number is K180118.

When was Arthrex NanoSuture Anchor approved by the FDA?

Arthrex NanoSuture Anchor received FDA 510(k) clearance on 2018-02-12, under approval number K180118.

What company makes Arthrex NanoSuture Anchor?

Arthrex NanoSuture Anchor is manufactured by Arthrex, Inc..

What is the FDA product code for Arthrex NanoSuture Anchor?

The FDA product code for Arthrex NanoSuture Anchor is MBI.

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Related Devices (Code: 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.