Orthosoft, Inc. dba Zimmer CAS
Orthosoft, Inc. dba Zimmer CAS appears in FDA public data with 7 recalls, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-0721-2022, Class II) was initiated on January 7, 2022.
Summary
- Total Recalls
- 7
- 510(k) Clearances
- 0
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-0721-2022 | Class II | NavitrackER Kit A: Knee, Model Number 20-8000-000-07, | January 7, 2022 |
| Z-1868-2017 | Class II | SmartTools Knee System Orthopedic Stereotaxic Instrument | February 20, 2017 |
| Z-1881-2017 | Class II | Navitrack System - OS Knee Universal, Orthopedic Stereotaxic Instrument CAS Software application in | October 6, 2011 |
| Z-2048-2017 | Class II | NDI P7 Position Sensor, Stereotaxic Instrument | June 9, 2009 |
| Z-2076-2017 | Class II | Navitrack System - OS Knee Universal, Stereotaxic instrument | October 28, 2008 |
| Z-2075-2017 | Class III | Navitrack¿ System - OS Knee Universal, Orthopedic Stereotaxic Instrument | June 20, 2008 |
| Z-2227-2017 | Class II | Sesamoid Plasty, Stereotaxic Instrument The Sesamoid Plasty workstation is used to run the tracking | June 4, 2008 |