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Stryker Trauma AG

FDA 510(k) & PMA Approved Devices — 12 products

Total Devices12
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K172210 ReUnion Reversible Fracture System (RFX), ReUnion Reverse Shoulder Arthroplasty System (RSA), ReUnion Total Shoulder Arthroplasty System (TSA)KWS2017-10-02 View
510(k) K133440 AXSOS 3 TI LOCKING PLATE SYSTEM LINE EXTENSIONHWC2013-12-18 View
510(k) K132502 VARIAX 2 SYSTEMHRS2013-10-23 View
510(k) K131365 T2 TIBIAL NAILING SYSTEMHSB2013-10-10 View
510(k) K130907 HOFFMANN LRF (LIMB RECONSTRUCTION FRAME) SYSTEMKTT2013-06-10 View
510(k) K131132 PELVIS II IMPLANT SYSTEMHRS2013-05-31 View
510(k) K130334 HOFFMANN LRF (LIMB RECONSTRUCTION FRAME SYSTEM)KTT2013-05-03 View
510(k) K123964 AXSOS 3 TI LOCKING PLATE SYSTEMHRS2013-03-28 View
510(k) K130009 VARIAX 2 COMPRESSION PLATING SYSTEMHRS2013-03-22 View
510(k) K123403 AXSOS PROXIMAL LATERAL TIBIA LONG PLATESHRS2013-03-20 View
510(k) K130116 SUPERIOR LATERAL VARIAX CLAVICLE PLATEHRS2013-03-05 View
510(k) K123401 GAMMA3 AND T2 RECON TARGETING DEVICESHSB2013-01-23 View
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