K-number	K860016
Device name	AESCULAP BONE MILL
Applicant	Aesculap Instruments Corp.
Product code	LYS
Device class	Class I
Decision date	Mar 19, 1986
Decision	Substantially Equivalent
Regulation	888.4540

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View the full FDA submission: accessdata.fda.gov

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AESCULAP BONE MILL

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