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Orthosoft, Inc. dba Zimmer CAS

4 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
Navitrack System - OS Knee Universal, Orthopedic Stereotaxic Instrument recall (Z-2075-2017)Orthosoft, Inc. dba Zimmer CAS2017-05-12
Navitrack System - OS Knee Universal, Stereotaxic instrument recall (Z-2076-2017)Orthosoft, Inc. dba Zimmer CAS2017-05-12
NDI P7 Position Sensor, Stereotaxic Instrument recall (Z-2048-2017)Orthosoft, Inc. dba Zimmer CAS2017-05-08
Navitrack System - OS Knee Universal, Orthopedic Stereotaxic Instrument CAS Software appli recall (Z-1881-2017)Orthosoft, Inc. dba Zimmer CAS2017-04-26

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