AOT & T-L Abutment
K-Number: K231874 · 2023-10-30
ApplicantTruabutment, Inc.
Decision Date2023-10-30
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
AOT & T-L Abutment is a medical device manufactured by Truabutment, Inc.. It received FDA 510(k) clearance on 2023-10-30 under approval number K231874. 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 AOT & T-L Abutment?
AOT & T-L Abutment is a medical device that received FDA 510(k) clearance on 2023-10-30. It is manufactured by Truabutment, Inc.. The 510(k) number is K231874.
When was AOT & T-L Abutment approved by the FDA?
AOT & T-L Abutment received FDA 510(k) clearance on 2023-10-30, under approval number K231874.
What company makes AOT & T-L Abutment?
AOT & T-L Abutment is manufactured by Truabutment, Inc..
What is the FDA product code for AOT & T-L Abutment?
The FDA product code for AOT & T-L 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.