K-number	K070323
Device name	TEMPORARY LIMB SALVAGE SHUNT
Applicant	Vascutek, Ltd.
Product code	DXC
Device class	Class II
Decision date	Feb 15, 2007
Decision	Substantially Equivalent
Regulation	870.4450

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View the full FDA submission: accessdata.fda.gov

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TEMPORARY LIMB SALVAGE SHUNT

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