K-number	K230416
Device name	Triathlon® Hinge Knee System; Triathlon® Revision Insert X3®
Applicant	Stryker
Product code	KRO
Device class	Class II
Decision date	May 19, 2023
Decision	Substantially Equivalent
Regulation	888.3510

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Source

View the full FDA submission: accessdata.fda.gov

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Triathlon® Hinge Knee System; Triathlon® Revision Insert X3®

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