K-number	K081401
Device name	MAYFIELD MR/X-RAY SKULL CLAMP
Applicant	Integra Lifesciences Corp.
Product code	HBL
Device class	Class II
Decision date	Oct 8, 2008
Decision	Substantially Equivalent
Regulation	882.4460

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View the full FDA submission: accessdata.fda.gov

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MAYFIELD MR/X-RAY SKULL CLAMP

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