K-number	K860356
Device name	ORTHOBLEND POWERED BONE MILL
Applicant	Zimmer, Inc.
Product code	LYS
Device class	Class I
Decision date	Jul 8, 1986
Decision	Substantially Equivalent
Regulation	888.4540

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View the full FDA submission: accessdata.fda.gov

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ORTHOBLEND POWERED BONE MILL

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