CreoDent Solidex Customized Abutment
K-Number: K202909 · 2021-04-02
ApplicantCreodent Prosthetics, Ltd.
Decision Date2021-04-02
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
CreoDent Solidex Customized Abutment is a medical device manufactured by Creodent Prosthetics, Ltd.. It received FDA 510(k) clearance on 2021-04-02 under approval number K202909. 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 CreoDent Solidex Customized Abutment?
CreoDent Solidex Customized Abutment is a medical device that received FDA 510(k) clearance on 2021-04-02. It is manufactured by Creodent Prosthetics, Ltd.. The 510(k) number is K202909.
When was CreoDent Solidex Customized Abutment approved by the FDA?
CreoDent Solidex Customized Abutment received FDA 510(k) clearance on 2021-04-02, under approval number K202909.
What company makes CreoDent Solidex Customized Abutment?
CreoDent Solidex Customized Abutment is manufactured by Creodent Prosthetics, Ltd..
What is the FDA product code for CreoDent Solidex Customized Abutment?
The FDA product code for CreoDent Solidex Customized 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.