FDA 510(k) Applications Submitted by DOUG STEINBERGER

FDA 510(k) Number Submission Date Device Name Applicant
K111266 05/04/2011 EASYLOCK OSTEOSYSTEM TRIMED, INC.
K112509 08/30/2011 TRIMED CLAVICLE FIXATION SYSTEM TRIMED, INC.
K212943 09/15/2021 SyntheCel Dura Repair Synthes (USA) products, LLC
K112794 09/26/2011 EOS SMALL BONE FIXATION SYSTEM TRIMED, INC.


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