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FDA 510(k)

Footmotion HammerToe

K-Number: K172485 · 2018-03-02

ApplicantNewclip Technics
Decision Date2018-03-02
Product CodeHTY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Footmotion HammerToe is the device name listed in this FDA 510(k) record. The listed applicant is Newclip Technics. It received FDA 510(k) clearance on 2018-03-02 under 510(k) number K172485. The device is classified under product code HTY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Footmotion HammerToe?

Footmotion HammerToe is a medical device that received FDA 510(k) clearance on 2018-03-02. The listed applicant is Newclip Technics. The 510(k) number is K172485.

When did Footmotion HammerToe receive FDA 510(k) clearance?

Footmotion HammerToe received FDA 510(k) clearance on 2018-03-02, under 510(k) number K172485.

Who is the listed applicant for Footmotion HammerToe?

The FDA 510(k) record lists Newclip Technics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Footmotion HammerToe?

The FDA product code for Footmotion HammerToe is HTY.

Other records listing Newclip Technics as applicant

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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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