K-number	K222912
Device name	c1Trac
Applicant	Zimmer Medizinsysteme GmbH
Product code	ITH
Device class	Class II
Decision date	May 16, 2023
Decision	Substantially Equivalent
Regulation	890.5900

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Source

View the full FDA submission: accessdata.fda.gov

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c1Trac

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