Stryker Trauma AG
FDA 510(k) medical device clearances.
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.