Stryker Trauma AG
Stryker Trauma AG holds FDA 510(k) medical device clearances, first cleared 2013, most recent 2017.
Top product codes for Stryker Trauma AG
Recent clearances by Stryker Trauma AG
- K172210 — ReUnion Reversible Fracture System (RFX), ReUnion Reverse Shoulder Arthroplasty System (RSA), ReUnion Total Shoulder Arthroplasty System (TSA)
- K153154 — Asnis JFX System
- K151178 — VariAx 2 Wrist Fusion System
- K143138 — AxSOS 3 Ti Locking Plate System
- K140961 — HOFFMANN LRF (LIMB RECONSTRUCTION FRAME) SYSTEM
- K141992 — VARIAX 2 SYSTEM
- K141677 — VARIAX ELBOW PLATING SYSTEM
- K141121 — AXSOS 3 TI LOCKING PLATE SYSTEM
- K141204 — VARIAX 2 ONE THIRD TUBULAR PLATING SYSTEM
- K140565 — VARIAX 2 COMPRESSION PLATING SYSTEM
- K140769 — VARIAX 2 SYSTEM
- K140376 — VARIAX 2 SYSTEM
- K140259 — VARIAX CLAVICLE HOOK PLATE
- K133451 — FIXOS SCREW SYSTEM
- K133440 — AXSOS 3 TI LOCKING PLATE SYSTEM LINE EXTENSION
- K132502 — VARIAX 2 SYSTEM
- K131365 — T2 TIBIAL NAILING SYSTEM
- K130907 — HOFFMANN LRF (LIMB RECONSTRUCTION FRAME) SYSTEM
- K131132 — PELVIS II IMPLANT SYSTEM
- K130334 — HOFFMANN LRF (LIMB RECONSTRUCTION FRAME SYSTEM)
- K123964 — AXSOS 3 TI LOCKING PLATE SYSTEM
- K130009 — VARIAX 2 COMPRESSION PLATING SYSTEM
- K123403 — AXSOS PROXIMAL LATERAL TIBIA LONG PLATES
- K130116 — SUPERIOR LATERAL VARIAX CLAVICLE PLATE
- K123401 — GAMMA3 AND T2 RECON TARGETING DEVICES
Data sourced from openFDA. This site is unofficial and independent of the FDA.