dS FootAnkle I6CH 1.5T Coil
K-Number: K162177 · 2016-09-14
ApplicantInvivo Corporation
Decision Date2016-09-14
Product CodeMOS
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
dS FootAnkle I6CH 1.5T Coil is a medical device manufactured by Invivo Corporation. It received FDA 510(k) clearance on 2016-09-14 under approval number K162177. The device is classified under product code MOS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the dS FootAnkle I6CH 1.5T Coil?
dS FootAnkle I6CH 1.5T Coil is a medical device that received FDA 510(k) clearance on 2016-09-14. It is manufactured by Invivo Corporation. The 510(k) number is K162177.
When was dS FootAnkle I6CH 1.5T Coil approved by the FDA?
dS FootAnkle I6CH 1.5T Coil received FDA 510(k) clearance on 2016-09-14, under approval number K162177.
What company makes dS FootAnkle I6CH 1.5T Coil?
dS FootAnkle I6CH 1.5T Coil is manufactured by Invivo Corporation.
What is the FDA product code for dS FootAnkle I6CH 1.5T Coil?
The FDA product code for dS FootAnkle I6CH 1.5T Coil is MOS.
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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.