Elos Accurate® Hybrid Base; Elos Accurate® Customized Abutment
K-Number: K241722 · 2024-09-13
ApplicantElos Medtech Pinol A/S
Decision Date2024-09-13
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Elos Accurate® Hybrid Base; Elos Accurate® Customized Abutment is a medical device manufactured by Elos Medtech Pinol A/S. It received FDA 510(k) clearance on 2024-09-13 under approval number K241722. 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 Elos Accurate® Hybrid Base; Elos Accurate® Customized Abutment?
Elos Accurate® Hybrid Base; Elos Accurate® Customized Abutment is a medical device that received FDA 510(k) clearance on 2024-09-13. It is manufactured by Elos Medtech Pinol A/S. The 510(k) number is K241722.
When was Elos Accurate® Hybrid Base; Elos Accurate® Customized Abutment approved by the FDA?
Elos Accurate® Hybrid Base; Elos Accurate® Customized Abutment received FDA 510(k) clearance on 2024-09-13, under approval number K241722.
What company makes Elos Accurate® Hybrid Base; Elos Accurate® Customized Abutment?
Elos Accurate® Hybrid Base; Elos Accurate® Customized Abutment is manufactured by Elos Medtech Pinol A/S.
What is the FDA product code for Elos Accurate® Hybrid Base; Elos Accurate® Customized Abutment?
The FDA product code for Elos Accurate® Hybrid Base; Elos Accurate® Customized Abutment is NHA.
Related Clinical Trials
Other Devices by Elos Medtech Pinol A/S
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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.