Footmotion Plating System
K-Number: K161448 · 2016-10-31
ApplicantNewclip Technics
Decision Date2016-10-31
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Footmotion Plating System is a medical device manufactured by Newclip Technics. It received FDA 510(k) clearance on 2016-10-31 under approval number K161448. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Footmotion Plating System?
Footmotion Plating System is a medical device that received FDA 510(k) clearance on 2016-10-31. It is manufactured by Newclip Technics. The 510(k) number is K161448.
When was Footmotion Plating System approved by the FDA?
Footmotion Plating System received FDA 510(k) clearance on 2016-10-31, under approval number K161448.
What company makes Footmotion Plating System?
Footmotion Plating System is manufactured by Newclip Technics.
What is the FDA product code for Footmotion Plating System?
The FDA product code for Footmotion Plating System is HRS.
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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.