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FDA 510(k) Applications Submitted by STUCKENBROCK MEDIZINTECHNIK GMBH
FDA 510(k) Number
Submission Date
Device Name
Applicant
K042902
10/20/2004
HERBERT ULNAR HEAD PROSTHESIS SYSTEM
STUCKENBROCK MEDIZINTECHNIK GMBH
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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