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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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