K-number	K041350
Device name	SYNTHES (USA) CHRONOS
Applicant	Synthes (Usa)
Product code	GXP
Device class	Class II
Decision date	Jul 8, 2004
Decision	Substantially Equivalent
Regulation	882.5300

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View the full FDA submission: accessdata.fda.gov

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SYNTHES (USA) CHRONOS

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