FDA 510(k) Applications Submitted by Fabian Stuckenbrock

FDA 510(k) Number Submission Date Device Name Applicant
K171624 06/02/2017 IXOS Radius Plate System Stuckenbrock Medizintechnik GmbH
K171628 06/02/2017 HBS2 Headless Bone Screw Stuckenbrock Medizintechnik GmbH


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