FDA 510(k) Applications Submitted by STRYKER CRANIOMAXILLOFACIAL

FDA 510(k) Number Submission Date Device Name Applicant
K092743 09/08/2009 THE LEIBINGER ADVANCE INTERNAL MIDFACE DISTRACTION SYSTEM STRYKER CRANIOMAXILLOFACIAL
K070876 03/29/2007 STRYKER TWIST DRILLS STRYKER CRANIOMAXILLOFACIAL


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