K-number	K955598
Device name	CLARUS SPINEPEN MODEL 2126
Applicant	Clarus Medical Systems, Inc.
Product code	GWG
Device class	Class II
Decision date	Feb 6, 1996
Decision	Substantially Equivalent
Regulation	882.1480

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View the full FDA submission: accessdata.fda.gov

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CLARUS SPINEPEN MODEL 2126

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