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FDA 510(k)

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 the device name listed in this FDA 510(k) record. The listed applicant is Cymedica Orthopedics, Inc.. It received FDA 510(k) clearance on 2023-03-22 under 510(k) 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. The listed applicant is Cymedica Orthopedics, Inc.. The 510(k) number is K230533.

When did Motive™ Electrode receive FDA 510(k) clearance?

Motive™ Electrode received FDA 510(k) clearance on 2023-03-22, under 510(k) number K230533.

Who is the listed applicant for Motive™ Electrode?

The FDA 510(k) record lists Cymedica Orthopedics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Motive™ Electrode?

The FDA product code for Motive™ Electrode is GXY.

Other records listing Cymedica Orthopedics, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K220738Motive Knee WrapK210604Intellihab SystemK163067CyMedica e-vive™ System; CY-1000

Related Devices (Code: GXY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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