K-number	K171769
Device name	Straumann PURE Ceramic Implants
Applicant	Straumann USA, LLC (On Behalf of Institut Straumann Ag)
Product code	DZE
Device class	Class II
Decision date	Nov 14, 2017
Decision	Substantially Equivalent
Regulation	872.3640

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View the full FDA submission: accessdata.fda.gov

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Straumann PURE Ceramic Implants

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