K-number	K101252
Device name	NEOTRACT ANCHOR SYSTEM MODEL: REF 11208
Applicant	Neotract, Inc.
Product code	GAT
Device class	Class II
Decision date	Jul 15, 2010
Decision	Substantially Equivalent
Regulation	878.5000

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View the full FDA submission: accessdata.fda.gov

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NEOTRACT ANCHOR SYSTEM MODEL: REF 11208

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