K-number	K920213
Device name	MITEK ANCHOR, MITEK ANCHOR II
Applicant	Mitek Surgical Products, Inc.
Product code	JDR
Device class	Class II
Decision date	May 1, 1992
Decision	Substantially Equivalent
Regulation	888.3030

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View the full FDA submission: accessdata.fda.gov

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MITEK ANCHOR, MITEK ANCHOR II

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