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.

Ignite Orthomotion

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

Total Devices2
Categories1
Latest Approval2025-09-02
TypeNumberDevice NameCodeDate
510(k) K251975 Achieve Partial Knee System - Porous Coated CoCrMo Femoral Component NJD 2025-09-02 View
510(k) K242307 ACHIEVE Partial Knee System NJD 2024-12-16 View