K-number	K033868
Device name	SYNTHES (USA) PATIENT SPECIFIC CRANIAL/CRANIOFACIAL IMPLANTS
Applicant	Synthes (Usa)
Product code	GXN
Device class	Class II
Decision date	Jun 21, 2004
Decision	Substantially Equivalent
Regulation	882.5330

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View the full FDA submission: accessdata.fda.gov

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SYNTHES (USA) PATIENT SPECIFIC CRANIAL/CRANIOFACIAL IMPLANTS

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