Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Spineway

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K231658 VEOS Spinal Fixation SystemNKB2023-10-10 View
510(k) K162694 Ayers Rock Cervical interbody fusion systemODP2017-01-12 View
↑