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FDA 510(k) Applications Submitted by Kara Budor
FDA 510(k) Number
Submission Date
Device Name
Applicant
K130986
04/09/2013
FRAG-LOC SYSTEM
ACUMED LLC
K131845
06/21/2013
ACUMED ANATOMIC RADIAL HEAD SYSTEM, ACUMED ANATOMIC RADIAL HEAD LONG STEMS, ACUMED ARH SLIDE-LOC
ACUMED LLC
K151886
07/09/2015
Acumed Ankle and Small Fragment Base Set Update
Acumed, LLC
K122538
08/21/2012
ACUMED PELVIC BONE PLATE SYSTEM
ACUMED LLC
K123890
12/18/2012
ACUMED CANNULATED SCREW SYSTEM
ACUMED LLC
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