FDA 510(k)

Arthrex Knotless SutureTak Anchor

K-Number: K171020 · 2017-05-16

Decision Date2017-05-16

Product CodeMBI

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

Arthrex Knotless SutureTak Anchor is a medical device manufactured by Arthrex, Inc.. It received FDA 510(k) clearance on 2017-05-16 under approval number K171020. 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 Knotless SutureTak Anchor?

Arthrex Knotless SutureTak Anchor is a medical device that received FDA 510(k) clearance on 2017-05-16. It is manufactured by Arthrex, Inc.. The 510(k) number is K171020.

When was Arthrex Knotless SutureTak Anchor approved by the FDA?

Arthrex Knotless SutureTak Anchor received FDA 510(k) clearance on 2017-05-16, under approval number K171020.

What company makes Arthrex Knotless SutureTak Anchor?

Arthrex Knotless SutureTak Anchor is manufactured by Arthrex, Inc..

What is the FDA product code for Arthrex Knotless SutureTak Anchor?

The FDA product code for Arthrex Knotless SutureTak 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.