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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