K-number	K862324
Device name	OSTEOGRAF/AR AND OSTEOGRAF/AR+
Applicant	Coors Biomedical Co.
Product code	LYC
Device class	Class II
Decision date	Aug 15, 1986
Decision	Substantially Equivalent
Regulation	872.3930

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View the full FDA submission: accessdata.fda.gov

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OSTEOGRAF/AR AND OSTEOGRAF/AR+

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