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FDA 510(k)

InnovaMatrix FS

K-Number: K210580 · 2021-04-21

ApplicantTriad Life Sciences, Inc.
Decision Date2021-04-21
Product CodeKGN
DecisionSubstantially Equivalent

Device Summary

InnovaMatrix FS is a medical device manufactured by Triad Life Sciences, Inc.. It received FDA 510(k) clearance on 2021-04-21 under approval number K210580. The device is classified under product code KGN. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the InnovaMatrix FS?

InnovaMatrix FS is a medical device that received FDA 510(k) clearance on 2021-04-21. It is manufactured by Triad Life Sciences, Inc.. The 510(k) number is K210580.

When was InnovaMatrix FS approved by the FDA?

InnovaMatrix FS received FDA 510(k) clearance on 2021-04-21, under approval number K210580.

What company makes InnovaMatrix FS?

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

What is the FDA product code for InnovaMatrix FS?

The FDA product code for InnovaMatrix FS is KGN.

Other Devices by Triad Life Sciences, Inc.

K193552InnovaMatrix K213716InnovaBurn K211902InnovaMatrix PD

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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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