Motive Electrode
K-Number: K230533 · 2023-03-22
ApplicantCymedica Orthopedics, Inc.
Decision Date2023-03-22
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
Motive Electrode is a medical device manufactured by Cymedica Orthopedics, Inc.. It received FDA 510(k) clearance on 2023-03-22 under approval number K230533. The device is classified under product code GXY. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Motive Electrode?
Motive Electrode is a medical device that received FDA 510(k) clearance on 2023-03-22. It is manufactured by Cymedica Orthopedics, Inc.. The 510(k) number is K230533.
When was Motive Electrode approved by the FDA?
Motive Electrode received FDA 510(k) clearance on 2023-03-22, under approval number K230533.
What company makes Motive Electrode?
Motive Electrode is manufactured by Cymedica Orthopedics, Inc..
What is the FDA product code for Motive Electrode?
The FDA product code for Motive Electrode is GXY.
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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.