K-number	K093897
Device name	SMITH & NEPHEW FOOTPRINT ULTRA PK SUTURE ANCHOR
Applicant	Smith & Nephew Inc., Endoscopy Div.
Product code	MBI
Device class	Class II
Decision date	Mar 4, 2010
Decision	Substantially Equivalent
Regulation	888.3040

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View the full FDA submission: accessdata.fda.gov

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SMITH & NEPHEW FOOTPRINT ULTRA PK SUTURE ANCHOR

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