FDA 510(k) Applications Submitted by Naviswiss AG

FDA 510(k) Number Submission Date Device Name Applicant
K223351 11/02/2022 Naviswiss Knee Naviswiss AG
K211429 05/07/2021 NAVIPLAN - CT Planning Software for Total Hip Replacement Naviswiss AG
K193094 11/07/2019 Naviswiss Hip Navigation System Naviswiss AG


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