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FDA 510(k)

SIMDA Abutment

K-Number: K223663 · 2023-05-24

ApplicantSimda Co., Ltd.
Decision Date2023-05-24
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SIMDA Abutment is a medical device manufactured by Simda Co., Ltd.. It received FDA 510(k) clearance on 2023-05-24 under approval number K223663. 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 SIMDA Abutment?

SIMDA Abutment is a medical device that received FDA 510(k) clearance on 2023-05-24. It is manufactured by Simda Co., Ltd.. The 510(k) number is K223663.

When was SIMDA Abutment approved by the FDA?

SIMDA Abutment received FDA 510(k) clearance on 2023-05-24, under approval number K223663.

What company makes SIMDA Abutment?

SIMDA Abutment is manufactured by Simda Co., Ltd..

What is the FDA product code for SIMDA Abutment?

The FDA product code for SIMDA Abutment is NHA.

Other Devices by Simda Co., Ltd.

K232271SIMDA abutment K252320SIMDA Abutments

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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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