K-number	K965135
Device name	LIFECORE CONICAL ABUTMENT
Applicant	Lifecore Biomedical, Inc.
Product code	DZE
Device class	Class II
Decision date	Feb 25, 1997
Decision	Substantially Equivalent
Regulation	872.3640

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View the full FDA submission: accessdata.fda.gov

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LIFECORE CONICAL ABUTMENT

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