K-number	K093090
Device name	GALILEOS IMPLANT, VERSION 1.7
Applicant	Sicat GmbH & Co. KG
Product code	LLZ
Device class	Class II
Decision date	Dec 17, 2009
Decision	Substantially Equivalent
Regulation	892.2050

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View the full FDA submission: accessdata.fda.gov

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GALILEOS IMPLANT, VERSION 1.7

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