FDA 510(k)

InnovaMatrix

K-Number: K193552 · 2020-10-21

Decision Date2020-10-21

Product CodeKGN

DecisionSubstantially Equivalent

Device Summary

InnovaMatrix is the device name listed in this FDA 510(k) record. The listed applicant is Triad Life Sciences, Inc.. It received FDA 510(k) clearance on 2020-10-21 under 510(k) number K193552. The device is classified under product code KGN. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the InnovaMatrix?

InnovaMatrix is a medical device that received FDA 510(k) clearance on 2020-10-21. The listed applicant is Triad Life Sciences, Inc.. The 510(k) number is K193552.

When did InnovaMatrix receive FDA 510(k) clearance?

InnovaMatrix received FDA 510(k) clearance on 2020-10-21, under 510(k) number K193552.

Who is the listed applicant for InnovaMatrix?

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

What is the FDA product code for InnovaMatrix?

The FDA product code for InnovaMatrix is KGN.

Other records listing Triad Life Sciences, 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.

K213716InnovaBurn K211902InnovaMatrix PD K210580InnovaMatrix FS

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.