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FDA 510(k) Applications for Medical Device Product Code "PBI"
FDA 510(k) Number
Applicant
Device Name
Decision Date
K121874
BIOMET MANUFACTURING CORP.
G7 ACETABULAR SYSTEM
11/23/2012
K212512
Zimmer, Inc.
G7« Vivacit-E« Freedom« Constrained Liner
04/28/2022
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