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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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