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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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