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FDA 510(k)

Phoenix Atherectomy System

K-Number: K182972 · 2018-12-20

Decision Date2018-12-20
Product CodeMCW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Phoenix Atherectomy System is a medical device manufactured by Volcano Atheromed, Inc.. It received FDA 510(k) clearance on 2018-12-20 under approval number K182972. The device is classified under product code MCW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Phoenix Atherectomy System?

Phoenix Atherectomy System is a medical device that received FDA 510(k) clearance on 2018-12-20. It is manufactured by Volcano Atheromed, Inc.. The 510(k) number is K182972.

When was Phoenix Atherectomy System approved by the FDA?

Phoenix Atherectomy System received FDA 510(k) clearance on 2018-12-20, under approval number K182972.

What company makes Phoenix Atherectomy System?

Phoenix Atherectomy System is manufactured by Volcano Atheromed, Inc..

What is the FDA product code for Phoenix Atherectomy System?

The FDA product code for Phoenix Atherectomy System is MCW.

Related Clinical Trials

Other Devices by Volcano Atheromed, Inc.

Related Devices (Code: MCW)

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.