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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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