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FDA 510(k)

MagnetOs

K-Number: K161859 · 2017-02-24

Decision Date2017-02-24
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MagnetOs is a medical device manufactured by Xpand Biotechnology BV. It received FDA 510(k) clearance on 2017-02-24 under approval number K161859. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MagnetOs?

MagnetOs is a medical device that received FDA 510(k) clearance on 2017-02-24. It is manufactured by Xpand Biotechnology BV. The 510(k) number is K161859.

When was MagnetOs approved by the FDA?

MagnetOs received FDA 510(k) clearance on 2017-02-24, under approval number K161859.

What company makes MagnetOs?

MagnetOs is manufactured by Xpand Biotechnology BV.

What is the FDA product code for MagnetOs?

The FDA product code for MagnetOs is MQV.

Related Devices (Code: MQV)

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.