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FDA 510(k)

MagnetOs

K-Number: K161859 · 2017-02-24

ApplicantXpand Biotechnology BV
Decision Date2017-02-24
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MagnetOs is the device name listed in this FDA 510(k) record. The listed applicant is Xpand Biotechnology BV. It received FDA 510(k) clearance on 2017-02-24 under 510(k) 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. The listed applicant is Xpand Biotechnology BV. The 510(k) number is K161859.

When did MagnetOs receive FDA 510(k) clearance?

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

Who is the listed applicant for MagnetOs?

The FDA 510(k) record lists Xpand Biotechnology BV as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MagnetOs?

The FDA product code for MagnetOs is MQV.

Related Devices (Code: MQV)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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.

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