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


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact