FDA 510(k)

Arthrex Corkscrew FT

K-Number: K173788 · 2018-03-01

Decision Date2018-03-01

Product CodeMAI

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

Arthrex Corkscrew FT is a medical device manufactured by Arthrex, Inc.. It received FDA 510(k) clearance on 2018-03-01 under approval number K173788. 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 Corkscrew FT?

Arthrex Corkscrew FT is a medical device that received FDA 510(k) clearance on 2018-03-01. It is manufactured by Arthrex, Inc.. The 510(k) number is K173788.

When was Arthrex Corkscrew FT approved by the FDA?

Arthrex Corkscrew FT received FDA 510(k) clearance on 2018-03-01, under approval number K173788.

What company makes Arthrex Corkscrew FT?

Arthrex Corkscrew FT is manufactured by Arthrex, Inc..

What is the FDA product code for Arthrex Corkscrew FT?

The FDA product code for Arthrex Corkscrew FT 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.