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Ortho Development Corp.

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5
Categories4
Latest FDA decision2025-12-19
TypeNumberDevice NameCodeDateActions
510(k) K253161 Balanced Knee System TriMax Porous Femoral ComponentsMBH2025-12-19 View
510(k) K251052 Trivicta® Hip StemMEH2025-05-22 View
510(k) K242984 BKS Revision SystemJWH2024-10-25 View
510(k) K242833 Legend® Acetabular ShellLPH2024-10-11 View
510(k) K233758 Trivicta™ Hip StemMEH2024-03-08 View
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