K-number	K780357
Device name	TITANIUM MULLER TOTAL HIP
Applicant	Biomet, Inc.
Product code	JDG
Device class	Class II
Decision date	Apr 5, 1978
Decision	Substantially Equivalent
Regulation	888.3360

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View the full FDA submission: accessdata.fda.gov

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TITANIUM MULLER TOTAL HIP

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