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FDA 510(k)

Motive Knee Wrap

K-Number: K220738 · 2022-05-12

ApplicantCymedica Orthopedics, Inc.
Decision Date2022-05-12
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Motive Knee Wrap is a medical device manufactured by Cymedica Orthopedics, Inc.. It received FDA 510(k) clearance on 2022-05-12 under approval number K220738. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Motive Knee Wrap?

Motive Knee Wrap is a medical device that received FDA 510(k) clearance on 2022-05-12. It is manufactured by Cymedica Orthopedics, Inc.. The 510(k) number is K220738.

When was Motive Knee Wrap approved by the FDA?

Motive Knee Wrap received FDA 510(k) clearance on 2022-05-12, under approval number K220738.

What company makes Motive Knee Wrap?

Motive Knee Wrap is manufactured by Cymedica Orthopedics, Inc..

What is the FDA product code for Motive Knee Wrap?

The FDA product code for Motive Knee Wrap is IPF.

Other Devices by Cymedica Orthopedics, Inc.

K163067CyMedica e-vive™ System; CY-1000 K210604Intellihab System K230533Motive™ Electrode

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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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