K-number	K043079
Device name	BICONTACT HIP SYSTEM WITH U-CAP
Applicant	Aesculap
Product code	MEH
Device class	Class II
Decision date	Dec 8, 2004
Decision	Substantially Equivalent
Regulation	888.3353

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View the full FDA submission: accessdata.fda.gov

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BICONTACT HIP SYSTEM WITH U-CAP

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