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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