FDA 510(k) Applications Submitted by SPINEWAY
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K152355 | 08/20/2015 | Twin Peaks Lumbar Interbody Fusion System | SPINEWAY |
| K150036 | 01/09/2015 | Blue Mountain Cervical Plate System | SPINEWAY |
| K150185 | 01/27/2015 | Mont Blanc Spinal System | SPINEWAY |
| K162694 | 09/27/2016 | Ayers Rock Cervical interbody fusion system | Spineway |
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