FDA 510(k) Applications Submitted by David Brumfield

FDA 510(k) Number Submission Date Device Name Applicant
K120597 02/28/2012 KOMPREDA CUSTOM SPINE, INC.
K173126 09/29/2017 ArisstosÖ Spinal System Ingenium Spine
K113361 11/14/2011 SECURIS SPINAL FIXATION CUMTOM SPINE


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