K-number	K934183
Device name	BONUTTI ANCHOR
Applicant	Apogee Medical Products, Inc.
Product code	MBI
Device class	Class II
Decision date	Apr 3, 1996
Decision	Substantially Equivalent for Some Indications
Regulation	888.3040

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Source

View the full FDA submission: accessdata.fda.gov

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BONUTTI ANCHOR

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