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Kico Knee Innovation Company Pty, Ltd.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories2
Latest Approval2025-01-13
TypeNumberDevice NameCodeDate
510(k) K243950 ARVIS® Shoulder SBF 2025-01-13 View
510(k) K242009 360CAS Knee OLO 2024-08-08 View