K-number	K110295
Device name	INTERLOCK-35 FIBERED IDC OCCLUSION SYSTEM
Applicant	Boston Scientific Corp
Product code	KRD
Device class	Class II
Decision date	Mar 3, 2011
Decision	Substantially Equivalent
Regulation	870.3300

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View the full FDA submission: accessdata.fda.gov

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INTERLOCK-35 FIBERED IDC OCCLUSION SYSTEM

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