K-number	K231915
Device name	Zfx Abutments
Applicant	Zfx GmbH - A Company of Zimvie
Product code	NHA
Device class	Class II
Decision date	Mar 1, 2024
Decision	Substantially Equivalent
Regulation	872.3630

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Source

View the full FDA submission: accessdata.fda.gov

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Zfx Abutments

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