K-number	K122353
Device name	CRAINFIX 2 TITANIUM CLAMP SYSTEM
Applicant	Aesculap, Inc.
Product code	GXN
Device class	Class II
Decision date	Aug 30, 2012
Decision	Substantially Equivalent
Regulation	882.5330

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View the full FDA submission: accessdata.fda.gov

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CRAINFIX 2 TITANIUM CLAMP SYSTEM

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