K-number	K083167
Device name	PHENIX CERVICAL INTERBODY DEVICE
Applicant	Spinal Devices, LLC
Product code	ODP
Device class	Class II
Decision date	Jan 13, 2009
Decision	Substantially Equivalent
Regulation	888.3080

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View the full FDA submission: accessdata.fda.gov

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PHENIX CERVICAL INTERBODY DEVICE

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