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FDA 510(k)

PRE-MILLED Abutment

K-Number: K202269 · 2020-11-25

ApplicantMit Global Co., Ltd.
Decision Date2020-11-25
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PRE-MILLED Abutment is a medical device manufactured by Mit Global Co., Ltd.. It received FDA 510(k) clearance on 2020-11-25 under approval number K202269. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRE-MILLED Abutment?

PRE-MILLED Abutment is a medical device that received FDA 510(k) clearance on 2020-11-25. It is manufactured by Mit Global Co., Ltd.. The 510(k) number is K202269.

When was PRE-MILLED Abutment approved by the FDA?

PRE-MILLED Abutment received FDA 510(k) clearance on 2020-11-25, under approval number K202269.

What company makes PRE-MILLED Abutment?

PRE-MILLED Abutment is manufactured by Mit Global Co., Ltd..

What is the FDA product code for PRE-MILLED Abutment?

The FDA product code for PRE-MILLED Abutment is NHA.

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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.

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