K-number	K981052
Device name	CRESCO TI IMPLANT CONCEPT
Applicant	Cresco TI Systems AB
Product code	DZE
Device class	Class II
Decision date	Dec 18, 2001
Decision	Substantially Equivalent
Regulation	872.3640

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View the full FDA submission: accessdata.fda.gov

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CRESCO TI IMPLANT CONCEPT

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