K-number	K191916
Device name	Stryker CMF MEDPOR Priority Customized Implant Kit
Applicant	Stryker Leibinger GmbH & Co KG
Product code	FWP
Device class	Class II
Decision date	Aug 15, 2019
Decision	Substantially Equivalent
Regulation	878.3550

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Source

View the full FDA submission: accessdata.fda.gov

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Stryker CMF MEDPOR Priority Customized Implant Kit

Everything you need for a 510(k) submission. Nothing you don't.