K-number	K082384
Device name	HAV-LOK BUNION CORRECTION SYSTEM
Applicant	Instratek, Inc.
Product code	HTN
Device class	Class II
Decision date	Dec 8, 2008
Decision	Substantially Equivalent
Regulation	888.3030

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View the full FDA submission: accessdata.fda.gov

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HAV-LOK BUNION CORRECTION SYSTEM

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