510(k) K071929 ยท HAW Neurological Stereotaxic Instrument
NAVITRACK SYSTEM- PARTIAL HIP RESURFACING UNIVERSAL
| Applicant | Orthosoft, Inc., Montreal, CA |
| Decision | Substantially Equivalent, Sep 19, 2007 |
| Received | Jul 13, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071929
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| May 8, 2017 | Orthosoft, Inc. dba Zimmer CAS NDI P7 Position Sensor, Stereotaxic Instrument Terminated |
HAW | None listed |
| Dec 22, 2009 | Zimmer Inc. Zimmer/CAS Power Cord, Sesamoid Plasty, NA, Zimmer/CAS, Montreal (Quebec), Canada; REF 20-8000-070-12. The device is the power cord component for the Sesamoid Plasty CAS workstation which connects th Terminated |
HAW | None listed |
| Jun 4, 2008 | Orthosoft, Inc. dba Zimmer CAS Sesamoid Plasty, Stereotaxic Instrument
The Sesamoid Plasty workstation is used to run the tracking software as part of the software based navigation systems. The affected Sesamoid Plasty components Terminated |
HAW | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.