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FDA 510(k)

InnovaMatrix PD

K-Number: K211902 · 2022-09-28

ApplicantTriad Life Sciences, Inc.
Decision Date2022-09-28
Product CodeKGN
DecisionSubstantially Equivalent

Device Summary

InnovaMatrix PD is a medical device manufactured by Triad Life Sciences, Inc.. It received FDA 510(k) clearance on 2022-09-28 under approval number K211902. The device is classified under product code KGN. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the InnovaMatrix PD?

InnovaMatrix PD is a medical device that received FDA 510(k) clearance on 2022-09-28. It is manufactured by Triad Life Sciences, Inc.. The 510(k) number is K211902.

When was InnovaMatrix PD approved by the FDA?

InnovaMatrix PD received FDA 510(k) clearance on 2022-09-28, under approval number K211902.

What company makes InnovaMatrix PD?

InnovaMatrix PD is manufactured by Triad Life Sciences, Inc..

What is the FDA product code for InnovaMatrix PD?

The FDA product code for InnovaMatrix PD is KGN.

Other Devices by Triad Life Sciences, Inc.

K193552InnovaMatrix K210580InnovaMatrix FS K213716InnovaBurn

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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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