K-number	K080153
Device name	SYNTHES (USA) CURVILINEAR DISTRACTION SYSTEM
Applicant	Synthes (Usa)
Product code	MQN
Device class	Class II
Decision date	May 14, 2008
Decision	Substantially Equivalent
Regulation	872.4760

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View the full FDA submission: accessdata.fda.gov

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SYNTHES (USA) CURVILINEAR DISTRACTION SYSTEM

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