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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