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FDA 510(k) Applications Submitted by Orthosoft d/b/a Zimmer CAS
FDA 510(k) Number
Submission Date
Device Name
Applicant
K230243
01/30/2023
ROSA« Knee System
Orthosoft d/b/a Zimmer CAS
K210121
01/19/2021
ROSA Partial Knee System
Orthosoft d/b/a Zimmer CAS
K221928
07/01/2022
ROSA« Knee System
Orthosoft d/b/a Zimmer CAS
K210653
03/04/2021
ONE Planner Hip
Orthosoft d/b/a Zimmer CAS
K210998
04/02/2021
ROSA Hip System
Orthosoft d/b/a Zimmer CAS
K213033
09/21/2021
iASSIST Knee System
Orthosoft d/b/a Zimmer CAS
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