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FDA 510(k)

Symphony Thrombectomy System

K-Number: K223216 · 2023-02-23

Decision Date2023-02-23
Product CodeQEW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Symphony Thrombectomy System is a medical device manufactured by Truvic Medical, Inc.. It received FDA 510(k) clearance on 2023-02-23 under approval number K223216. The device is classified under product code QEW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Symphony Thrombectomy System?

Symphony Thrombectomy System is a medical device that received FDA 510(k) clearance on 2023-02-23. It is manufactured by Truvic Medical, Inc.. The 510(k) number is K223216.

When was Symphony Thrombectomy System approved by the FDA?

Symphony Thrombectomy System received FDA 510(k) clearance on 2023-02-23, under approval number K223216.

What company makes Symphony Thrombectomy System?

Symphony Thrombectomy System is manufactured by Truvic Medical, Inc..

What is the FDA product code for Symphony Thrombectomy System?

The FDA product code for Symphony Thrombectomy System is QEW.

Related Clinical Trials

Other Devices by Truvic Medical, Inc.

Related Devices (Code: QEW)

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.