FDA 510(k)

Mimics inPrint

K-Number: K173619 · 2018-03-21

Decision Date2018-03-21

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

Mimics inPrint is a medical device manufactured by Materialise NV. It received FDA 510(k) clearance on 2018-03-21 under approval number K173619. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Mimics inPrint?

Mimics inPrint is a medical device that received FDA 510(k) clearance on 2018-03-21. It is manufactured by Materialise NV. The 510(k) number is K173619.

When was Mimics inPrint approved by the FDA?

Mimics inPrint received FDA 510(k) clearance on 2018-03-21, under approval number K173619.

What company makes Mimics inPrint?

Mimics inPrint is manufactured by Materialise NV.

What is the FDA product code for Mimics inPrint?

The FDA product code for Mimics inPrint is LLZ.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.