FDA 510(k) Applications Submitted by Andrew "Drew" Johnson

FDA 510(k) Number Submission Date Device Name Applicant
K980367 01/29/1998 AEROSET SYSTEM ABBOTT LABORATORIES
K202105 07/29/2020 OsteoMed ExtremiFix Mini & Small System Tray OsteoMed LLC
K203479 11/27/2020 ExtremiLOCK Lateral Ankle Fusion Plates OsteoMed
K974779 12/22/1997 ABBOTT ALCYON(TM) 300 (WITHOUT ISE MODULE) AND 300I (WITH ISE MODULE) ANALYZER ABBOTT LABORATORIES
K202680 09/15/2020 OsteoMed ExtremiFix Mini & Small Cannulated Screw System OsteoMed LLC


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