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.

Next Orthosurgical

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4
Categories3
Latest Approval2024-09-19
TypeNumberDevice NameCodeDate
510(k) K242509 HAnano InterFuse(R) Modular Interbody MAX 2024-09-19 View
510(k) K190981 NEX-D2 Posterior Fixation System NKB 2020-01-15 View
510(k) K161608 InterForm Cervical Interbody Cage System ODP 2016-09-30 View
510(k) K161499 VertiForm Posterior Fixation System NKB 2016-07-29 View