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FDA 510(k)

ExoToe Staple

K-Number: K172205 · 2018-01-11

ApplicantExotoe, LLC
Decision Date2018-01-11
Product CodeJDR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ExoToe Staple is a medical device manufactured by Exotoe, LLC. It received FDA 510(k) clearance on 2018-01-11 under approval number K172205. The device is classified under product code JDR. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ExoToe Staple?

ExoToe Staple is a medical device that received FDA 510(k) clearance on 2018-01-11. It is manufactured by Exotoe, LLC. The 510(k) number is K172205.

When was ExoToe Staple approved by the FDA?

ExoToe Staple received FDA 510(k) clearance on 2018-01-11, under approval number K172205.

What company makes ExoToe Staple?

ExoToe Staple is manufactured by Exotoe, LLC.

What is the FDA product code for ExoToe Staple?

The FDA product code for ExoToe Staple is JDR.

Related Devices (Code: JDR)

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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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