K-number	K040864
Device name	CRANIOFIX AND CRANIOFIX2 TITANIUM CLAMP SYSTEM
Applicant	Aesculap
Product code	GXN
Device class	Class II
Decision date	Jun 17, 2004
Decision	Substantially Equivalent
Regulation	882.5330

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View the full FDA submission: accessdata.fda.gov

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CRANIOFIX AND CRANIOFIX2 TITANIUM CLAMP SYSTEM

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