Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Naviswiss AG

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories2
Latest Approval2023-01-31
TypeNumberDevice NameCodeDate
510(k) K223351 Naviswiss Knee OLO 2023-01-31 View
510(k) K211429 NAVIPLAN - CT Planning Software for Total Hip Replacement LLZ 2021-10-05 View
510(k) K193094 Naviswiss Hip Navigation System OLO 2020-06-10 View