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FDA 510(k)

MVP Aligner System

K-Number: K193130 · 2020-08-07

Decision Date2020-08-07
Product CodeNXC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MVP Aligner System is a medical device manufactured by Mvp Aligners, LLC. It received FDA 510(k) clearance on 2020-08-07 under approval number K193130. The device is classified under product code NXC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MVP Aligner System?

MVP Aligner System is a medical device that received FDA 510(k) clearance on 2020-08-07. It is manufactured by Mvp Aligners, LLC. The 510(k) number is K193130.

When was MVP Aligner System approved by the FDA?

MVP Aligner System received FDA 510(k) clearance on 2020-08-07, under approval number K193130.

What company makes MVP Aligner System?

MVP Aligner System is manufactured by Mvp Aligners, LLC.

What is the FDA product code for MVP Aligner System?

The FDA product code for MVP Aligner System is NXC.

Related Clinical Trials

Related Devices (Code: NXC)

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.