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

Spine Innovation, LLC

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

Total Devices2
Categories1
Latest Approval2026-01-08
TypeNumberDevice NameCodeDate
510(k) K253266 Titanium Interbody System MAX 2026-01-08 View
510(k) K153356 Spine Innovation Interbody System MAX 2016-01-14 View
↑