K-number	K203488
Device name	emField
Applicant	Zimmer Medizinsysteme GmbH
Product code	IPF
Device class	Class II
Decision date	Feb 19, 2021
Decision	Substantially Equivalent
Regulation	890.5850

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Source

View the full FDA submission: accessdata.fda.gov

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emField

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