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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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