Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

InnovaMatrix

K-Number: K193552 · 2020-10-21

Decision Date2020-10-21
Product CodeKGN
DecisionSubstantially Equivalent

Device Summary

InnovaMatrix is a medical device manufactured by Triad Life Sciences, Inc.. It received FDA 510(k) clearance on 2020-10-21 under approval 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. It is manufactured by Triad Life Sciences, Inc.. The 510(k) number is K193552.

When was InnovaMatrix approved by the FDA?

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

What company makes InnovaMatrix?

InnovaMatrix is manufactured by Triad Life Sciences, Inc..

What is the FDA product code for InnovaMatrix?

The FDA product code for InnovaMatrix is KGN.

Other Devices by Triad Life Sciences, Inc.

Related Devices (Code: KGN)

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.