K-number	K032064
Device name	THEKEN CPOD/LPOD VERTEBRAL BODY REPLACEMENT SYSTEM
Applicant	Theken Surgical,Llc
Product code	MQP
Device class	Class II
Decision date	Feb 20, 2004
Decision	Substantially Equivalent
Regulation	888.3060

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Source

View the full FDA submission: accessdata.fda.gov

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THEKEN CPOD/LPOD VERTEBRAL BODY REPLACEMENT SYSTEM

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