FDA 510(k)

Arthrex FibuLock Nail

K-Number: K173656 · 2018-07-26

Decision Date2018-07-26

Product CodeHSB

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

Arthrex FibuLock Nail is a medical device manufactured by Arthrex, Inc.. It received FDA 510(k) clearance on 2018-07-26 under approval number K173656. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Arthrex FibuLock Nail?

Arthrex FibuLock Nail is a medical device that received FDA 510(k) clearance on 2018-07-26. It is manufactured by Arthrex, Inc.. The 510(k) number is K173656.

When was Arthrex FibuLock Nail approved by the FDA?

Arthrex FibuLock Nail received FDA 510(k) clearance on 2018-07-26, under approval number K173656.

What company makes Arthrex FibuLock Nail?

Arthrex FibuLock Nail is manufactured by Arthrex, Inc..

What is the FDA product code for Arthrex FibuLock Nail?

The FDA product code for Arthrex FibuLock Nail is HSB.

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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.