K-number	K123232
Device name	SPINEOLOGY SPINOUS PROCESS PLATE
Applicant	Spineology, Inc.
Product code	KWP
Device class	Class II
Decision date	Feb 7, 2013
Decision	Substantially Equivalent
Regulation	888.3050

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Source

View the full FDA submission: accessdata.fda.gov

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SPINEOLOGY SPINOUS PROCESS PLATE

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