Orthosoft, Inc. dba Zimmer CAS

FDA Regulatory Profile

Summary

Total Recalls
7
510(k) Clearances
0
Inspections
0
Compliance Actions
1

Known Names

orthosoft, inc. dba zimmer cas, orthosoft inc. (d/b/a) zimmer cas), orthosoft inc (d/b/a zimmer cas), orthosoft inc. (d/b/a) zimmer cas

Recent Recalls

NumberClassProductDate
Z-0721-2022Class IINavitrackER Kit A: Knee, Model Number 20-8000-000-07,January 7, 2022
Z-1868-2017Class IISmartTools Knee System Orthopedic Stereotaxic InstrumentFebruary 20, 2017
Z-1881-2017Class IINavitrack System - OS Knee Universal, Orthopedic Stereotaxic Instrument CAS Software application inOctober 6, 2011
Z-2048-2017Class IINDI P7 Position Sensor, Stereotaxic InstrumentJune 9, 2009
Z-2076-2017Class IINavitrack System - OS Knee Universal, Stereotaxic instrumentOctober 28, 2008
Z-2075-2017Class IIINavitrack¿ System - OS Knee Universal, Orthopedic Stereotaxic InstrumentJune 20, 2008
Z-2227-2017Class IISesamoid Plasty, Stereotaxic Instrument The Sesamoid Plasty workstation is used to run the trackingJune 4, 2008