K-number	K041115
Device name	GII QUICKANCHOR PLUS
Applicant	Depuy Mitek, A Johnson & Johnson Company
Product code	JDR
Device class	Class II
Decision date	May 28, 2004
Decision	Substantially Equivalent
Regulation	888.3030

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Source

View the full FDA submission: accessdata.fda.gov

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GII QUICKANCHOR PLUS

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