FDA 510(k) Applications Submitted by b-One Ortho, Corp.

FDA 510(k) Number Submission Date Device Name Applicant
K210483 02/19/2021 MOBIO Total Knee System b-ONE ORTHO, Corp.
K222431 08/11/2022 b-ONER MOBIO Total Knee System b-ONE ORTHO, Corp.
K202429 08/25/2020 Mobio Total Knee System b-One Ortho, Corp.
K213673 11/22/2021 b-ONE MOBIO Total Knee System b-ONE ORTHO, Corp.


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