K-number	K241722
Device name	Elos Accurate® Hybrid Base; Elos Accurate® Customized Abutment
Applicant	Elos Medtech Pinol A/S
Product code	NHA
Device class	Class II
Decision date	Sep 13, 2024
Decision	Substantially Equivalent
Regulation	872.3630

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Source

View the full FDA submission: accessdata.fda.gov

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Elos Accurate® Hybrid Base; Elos Accurate® Customized Abutment

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Elos Accurate® Hybrid Base; Elos Accurate® Customized Abutment