FDA 510(k) Applications Submitted by Biomet Orthopedics

FDA 510(k) Number Submission Date Device Name Applicant
K223631 12/05/2022 Comprehensive Segmental Revision System(SRS) Biomet Orthopedics
K200196 01/27/2020 Taperloc« Complete Hip Stems Biomet Orthopedics


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