FDA 510(k) Applications Submitted by Grace Johnson-Bann

FDA 510(k) Number	Submission Date	Device Name	Applicant
K170288	01/30/2017	BIOFOAM« Additive Manufacturing (BIOFOAM« AM), ADVANCE« BIOFOAM« Tibial Base, EVOLUTION« BIOFOAM« Tibial Base, DYNASTY« BIOFOAM« Acetabular Shell	MicroPort Orthopedics, Inc.
K180317	02/05/2018	EVOLUTION« Knee Systems û MR Labeling, EVOLUTION« BIOFOAM« Tibial System, EVOLUTION« Revision Tibial System, EVOLUTION« Revision CCK System	MicroPort Orthopedics, Inc.