Orthosoft, Inc. dba Zimmer CAS
4 FDA 510(k) clearances · Recalling firm
◉ Watch Orthosoft, Inc. dba Zimmer CAS
| Record | Firm | Date |
|---|---|---|
| Navitrack System - OS Knee Universal, Orthopedic Stereotaxic Instrument recall (Z-2075-2017) | Orthosoft, Inc. dba Zimmer CAS | 2017-05-12 |
| Navitrack System - OS Knee Universal, Stereotaxic instrument recall (Z-2076-2017) | Orthosoft, Inc. dba Zimmer CAS | 2017-05-12 |
| NDI P7 Position Sensor, Stereotaxic Instrument recall (Z-2048-2017) | Orthosoft, Inc. dba Zimmer CAS | 2017-05-08 |
| Navitrack System - OS Knee Universal, Orthopedic Stereotaxic Instrument CAS Software appli recall (Z-1881-2017) | Orthosoft, Inc. dba Zimmer CAS | 2017-04-26 |
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Every clearance here is in the API, with alerts when new ones post.