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Stryker Corporation (Tornier, S.A.S.)

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

Total Devices2
Categories1
Latest FDA decision2026-04-03
TypeNumberDevice NameCodeDateActions
510(k) K253674 Blueprint Patient-Specific InstrumentationPHX2026-04-03 View
510(k) K241491 Blueprint Patient-Specific Instrumentation; Shoulder iD Primary Reversed GlenoidPHX2024-10-10 View
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