K-number	K060271
Device name	SPIRALOK ANCHOR
Applicant	Depuy Mitek, A Johnson & Johnson Company
Product code	HWC
Device class	Class II
Decision date	May 4, 2006
Decision	Substantially Equivalent
Regulation	888.3040

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Source

View the full FDA submission: accessdata.fda.gov

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SPIRALOK ANCHOR

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