K-number	K121153
Device name	PEEK CUSTOMIZED CRAIAL IMPLANT KIT
Applicant	Stryker
Product code	GWO
Device class	Class II
Decision date	Sep 14, 2012
Decision	Substantially Equivalent
Regulation	882.5320

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Source

View the full FDA submission: accessdata.fda.gov

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PEEK CUSTOMIZED CRAIAL IMPLANT KIT

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