510(k) K140259

VARIAX CLAVICLE HOOK PLATE by Stryker Trauma AG — Product Code HRS

K140259 is an FDA 510(k) premarket notification submitted by Stryker Trauma AG for the device "VARIAX CLAVICLE HOOK PLATE". The FDA issued a decision of Substantially Equivalent on Apr 1, 2014. The device falls under product code HRS (Plate, Fixation, Bone), a Class II device regulated under 21 CFR 888.3030. Stryker Trauma AG has 31 other 510(k) clearances on record.