K-number	K021850
Device name	SYNTHES (USA) 1.3 MM CRANIOFACIAL SCREWS
Applicant	Synthes (Usa)
Product code	DZL
Device class	Class II
Decision date	Jun 10, 2002
Decision	Substantially Equivalent
Regulation	872.4880

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View the full FDA submission: accessdata.fda.gov

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SYNTHES (USA) 1.3 MM CRANIOFACIAL SCREWS

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