K-number	K915089
Device name	MITEK QUICKANCHOR(TM), MODIFICATION
Applicant	Mitek Surgical Products, Inc.
Product code	GAS
Device class	Class II
Decision date	Feb 3, 1992
Decision	Substantially Equivalent
Regulation	878.5000

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View the full FDA submission: accessdata.fda.gov

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MITEK QUICKANCHOR(TM), MODIFICATION

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