K-number	K060707
Device name	AESCULAP BIPOLAR ACETABULAR CUP
Applicant	Aesculap, Inc.
Product code	KWY
Device class	Class II
Decision date	May 31, 2006
Decision	Substantially Equivalent
Regulation	888.3390

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View the full FDA submission: accessdata.fda.gov

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AESCULAP BIPOLAR ACETABULAR CUP

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