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 a medical device manufactured by Newclip Technics. It received FDA 510(k) clearance on 2018-03-02 under approval 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. It is manufactured by Newclip Technics. The 510(k) number is K172485.
When was Footmotion HammerToe approved by the FDA?
Footmotion HammerToe received FDA 510(k) clearance on 2018-03-02, under approval number K172485.
What company makes Footmotion HammerToe?
Footmotion HammerToe is manufactured by Newclip Technics.
What is the FDA product code for Footmotion HammerToe?
The FDA product code for Footmotion HammerToe is HTY.
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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.