K-number	K062920
Device name	ORTHOFIX TITANIUM HUMERAL PLATING SYSTEM LSP
Applicant	Orthofix Srl
Product code	KTW
Device class	Class II
Decision date	Nov 13, 2006
Decision	Substantially Equivalent
Regulation	888.3030

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Source

View the full FDA submission: accessdata.fda.gov

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ORTHOFIX TITANIUM HUMERAL PLATING SYSTEM LSP

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