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.

Orthosoft Inc. (d/b/a) Zimmer CAS

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories2
Latest Approval2026-02-04
TypeNumberDevice NameCodeDate
510(k) K260104 Signature™ ONE System QHE 2026-02-04 View
510(k) K251314 Rosa® Knee System OLO 2025-11-13 View
510(k) K242864 ROSA® Knee System OLO 2024-10-18 View
↑