K-number	K023884
Device name	MODIFICATION ORIA SPINAL SYSTEM
Applicant	Ortho Tec, LLC
Product code	KWP
Device class	Class II
Decision date	Aug 20, 2003
Decision	Substantially Equivalent
Regulation	888.3050

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Source

View the full FDA submission: accessdata.fda.gov

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MODIFICATION ORIA SPINAL SYSTEM

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