510(k) K071714 ยท HAW Neurological Stereotaxic Instrument
NAVITRACK SYSTEM - OS UNICONDYLAR KNEE UNIVERSAL, MODEL# PRO-06003
| Applicant | Orthosoft, Inc., Montreal, CA |
| Decision | Substantially Equivalent, Jul 20, 2007 |
| Received | Jun 22, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K071714
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| 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 |
| Mar 2, 2009 | Zimmer Inc. Orthosoft Navitrack, OS Unicondylar Knee 1.0 - Universal; software application for orthopedic surgical stereotaxic instrument. Terminated |
HAW | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.