K-number	K132042
Device name	AMB101 SYSTEM, AMBLYZ, LCG SYSTEM, XPAND
Applicant	X6d, Ltd.
Product code	HOY
Device class	Class I
Decision date	Apr 28, 2014
Decision	Substantially Equivalent
Regulation	886.4750

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View the full FDA submission: accessdata.fda.gov

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AMB101 SYSTEM, AMBLYZ, LCG SYSTEM, XPAND

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