K-number	K982320
Device name	DEPUY MOTECH MOSS MIAMI SPINAL SYSTEM
Applicant	Depuy, Inc.
Product code	KWP
Device class	Class II
Decision date	Sep 14, 1998
Decision	Substantially Equivalent
Regulation	888.3050

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View the full FDA submission: accessdata.fda.gov

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DEPUY MOTECH MOSS MIAMI SPINAL SYSTEM

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