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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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