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FDA 510(k)

MyndMove, MyndMove 2.0

K-Number: K233006 · 2024-06-25

ApplicantMyndtec, Inc.
Decision Date2024-06-25
Product CodeGZI
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MyndMove, MyndMove 2.0 is a medical device manufactured by Myndtec, Inc.. It received FDA 510(k) clearance on 2024-06-25 under approval number K233006. The device is classified under product code GZI. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MyndMove, MyndMove 2.0?

MyndMove, MyndMove 2.0 is a medical device that received FDA 510(k) clearance on 2024-06-25. It is manufactured by Myndtec, Inc.. The 510(k) number is K233006.

When was MyndMove, MyndMove 2.0 approved by the FDA?

MyndMove, MyndMove 2.0 received FDA 510(k) clearance on 2024-06-25, under approval number K233006.

What company makes MyndMove, MyndMove 2.0?

MyndMove, MyndMove 2.0 is manufactured by Myndtec, Inc..

What is the FDA product code for MyndMove, MyndMove 2.0?

The FDA product code for MyndMove, MyndMove 2.0 is GZI.

Other Devices by Myndtec, Inc.

K170564MyndMove System, MyndMove Functional Electrical Stimulator K212149MyndMove 2.0

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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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