K-number	K911936
Device name	OSTEOMED SBF SYSTEM (SBF)
Applicant	Osteomed Corp.
Product code	DZL
Device class	Class II
Decision date	Aug 21, 1991
Decision	Substantially Equivalent
Regulation	872.4880

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View the full FDA submission: accessdata.fda.gov

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OSTEOMED SBF SYSTEM (SBF)

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