K-number	K990295
Device name	BONE ANCHOR SYSTEM III (BAS III)
Applicant	Boston Scientific Corp
Product code	MBI
Device class	Class II
Decision date	Mar 5, 1999
Decision	Substantially Equivalent
Regulation	888.3040

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View the full FDA submission: accessdata.fda.gov

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BONE ANCHOR SYSTEM III (BAS III)

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