Spineway - FDA 510(k) Cleared Devices
Recent clearances: VEOS Spinal Fixation System, Ayers Rock Cervical interbody fusion system, Twin Peaks Lumbar Interbody Fusion System
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Spineway Orthopedic ✕
5 devices
Cleared
Oct 10, 2023
VEOS Spinal Fixation System
Orthopedic
125d
Cleared
Jan 12, 2017
Ayers Rock Cervical interbody fusion system
Orthopedic
107d
Cleared
Dec 10, 2015
Twin Peaks Lumbar Interbody Fusion System
Orthopedic
112d
Cleared
May 12, 2015
Mont Blanc Spinal System
Orthopedic
105d
Cleared
May 07, 2015
Blue Mountain Cervical Plate System
Orthopedic
118d