K-number	K152076
Device name	PEEK Customized Cranial Implant, PEEK Customized Cranial Implant Priority
Applicant	Stryker
Product code	GWO
Device class	Class II
Decision date	Aug 26, 2015
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 Cranial Implant, PEEK Customized Cranial Implant Priority

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