K-number	K212512
Device name	G7® Vivacit-E® Freedom® Constrained Liner
Applicant	Zimmer, Inc.
Product code	PBI
Device class	Class II
Decision date	Apr 28, 2022
Decision	Substantially Equivalent
Regulation	888.3310

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Source

View the full FDA submission: accessdata.fda.gov

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G7® Vivacit-E® Freedom® Constrained Liner

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