K-number	K002592
Device name	INTERPORE CROSS ANTERIOR CERVICAL PLATE SYSTEM
Applicant	Interpore Cross Intl.
Product code	KWQ
Device class	Class II
Decision date	Oct 6, 2000
Decision	Substantially Equivalent
Regulation	888.3060

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View the full FDA submission: accessdata.fda.gov

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INTERPORE CROSS ANTERIOR CERVICAL PLATE SYSTEM

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