510(k) K060336 ยท HAW Neurological Stereotaxic Instrument
NAVITRACK SYSTEM-OS KNEE UNIVERSAL, MODEL PRO-05002
| Applicant | Orthosoft, Inc., Montreal, CA |
| Decision | Substantially Equivalent, Apr 28, 2006 |
| Received | Feb 10, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K060336
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| May 12, 2017 | Orthosoft, Inc. dba Zimmer CAS Navitrack System - OS Knee Universal, Stereotaxic instrument Terminated |
HAW | None listed |
| May 12, 2017 | Orthosoft, Inc. dba Zimmer CAS Navitrack System - OS Knee Universal, Orthopedic 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 |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.