K-number	K102401
Device name	HEMI IMPLANT; MINI HEMI IMPLANT
Applicant	Vilex, Inc.
Product code	KWD
Device class	Class II
Decision date	Jul 20, 2011
Decision	Substantially Equivalent
Regulation	888.3730

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View the full FDA submission: accessdata.fda.gov

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HEMI IMPLANT; MINI HEMI IMPLANT

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