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FDA 510(k) Applications Submitted by Axis Orthopaedics
FDA 510(k) Number
Submission Date
Device Name
Applicant
K180301
02/02/2018
AXIS 5.5 Lumbar Pedicle Screw System
Axis Orthopaedics
K181140
04/30/2018
Axis Chena Cervical PEEK Spacer System
Axis Orthopaedics
K173867
12/20/2017
Axis Anterior Cervical Plate System
Axis Orthopaedics
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