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FDA 510(k)

Preat Abutments

K-Number: K220823 · 2022-10-26

ApplicantPreat Corporation
Decision Date2022-10-26
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Preat Abutments is a medical device manufactured by Preat Corporation. It received FDA 510(k) clearance on 2022-10-26 under approval number K220823. 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 Preat Abutments?

Preat Abutments is a medical device that received FDA 510(k) clearance on 2022-10-26. It is manufactured by Preat Corporation. The 510(k) number is K220823.

When was Preat Abutments approved by the FDA?

Preat Abutments received FDA 510(k) clearance on 2022-10-26, under approval number K220823.

What company makes Preat Abutments?

Preat Abutments is manufactured by Preat Corporation.

What is the FDA product code for Preat Abutments?

The FDA product code for Preat Abutments is NHA.

Other Devices by Preat Corporation

K183518Preat Abutments K243824Preat 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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