FDA 510(k) Applications Submitted by Kavina Veeren

FDA 510(k) Number Submission Date Device Name Applicant
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


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