Orthosoft Inc (D/B/A Zimmer Cas)
Orthosoft Inc (D/B/A Zimmer Cas) holds FDA 510(k) medical device clearances, first cleared 2017, most recent 2026.
Name variants for Orthosoft Inc (D/B/A Zimmer Cas)
as filed with FDA- Orthosoft Inc (D/B/A Zimmer Cas)
- Orthosoft Inc. (d/b/a) Zimmer CAS
- Orthosoft Inc. (D/B/A) Zimmer Cas)
Top product codes for Orthosoft Inc (D/B/A Zimmer Cas)
Recent clearances by Orthosoft Inc (D/B/A Zimmer Cas)
- K261510 — Signature ONE System
- K260582 — ROSA® Shoulder System
- K260104 — Signature ONE System
- K251314 — Rosa® Knee System
- K242864 — ROSA® Knee System
- K233199 — ROSA® Shoulder System
- K232425 — Signature ONE System
- K230567 — OptiVu ROSA® MxR
- K231162 — ROSA Hip System
- K230180 — Rosa Knee System
- K220733 — OptiVu ROSA MxR
- K213708 — ROSA® Knee System
- K212560 — Signature ONE System
- K200615 — Signature ONE System
- K192080 — iASSIST Knee System
- K192074 — Signature ONE System
- K183544 — Efficient Care 3D Planning
- K190595 — Signature ONE System
- K182964 — ROSA Knee System
- K171269 — X-PSI Knee System
Data sourced from openFDA. This site is unofficial and independent of the FDA.