K-number	K043229
Device name	MODIFICATION TO ALTIUS OCT SYSTEM
Applicant	Interpore Cross Intl.
Product code	KWP
Device class	Class II
Decision date	Dec 21, 2004
Decision	Substantially Equivalent
Regulation	888.3050

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO ALTIUS OCT SYSTEM

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