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Spineway

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories2
Latest Approval2023-10-10
TypeNumberDevice NameCodeDate
510(k) K231658 VEOS Spinal Fixation System NKB 2023-10-10 View
510(k) K162694 Ayers Rock Cervical interbody fusion system ODP 2017-01-12 View
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