K-number	K162341
Device name	Stryker OrthoMap Precision Knee system
Applicant	Stryker Leibinger GmbH & Co KG
Product code	OLO
Device class	Class II
Decision date	Oct 12, 2016
Decision	Substantially Equivalent
Regulation	882.4560

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Source

View the full FDA submission: accessdata.fda.gov

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Stryker OrthoMap Precision Knee system

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