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FDA 510(k)

Symphony

K-Number: K200413 · 2020-07-29

ApplicantAroa Biosurgery , Ltd.
Decision Date2020-07-29
Product CodeKGN
DecisionSubstantially Equivalent

Device Summary

Symphony is a medical device manufactured by Aroa Biosurgery , Ltd.. It received FDA 510(k) clearance on 2020-07-29 under approval number K200413. The device is classified under product code KGN. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Symphony?

Symphony is a medical device that received FDA 510(k) clearance on 2020-07-29. It is manufactured by Aroa Biosurgery , Ltd.. The 510(k) number is K200413.

When was Symphony approved by the FDA?

Symphony received FDA 510(k) clearance on 2020-07-29, under approval number K200413.

What company makes Symphony?

Symphony is manufactured by Aroa Biosurgery , Ltd..

What is the FDA product code for Symphony?

The FDA product code for Symphony is KGN.

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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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