510(k) K072368 ยท HSX Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer
CONFORMIS METAL BACKED TIBIAL COMPONENT
| Applicant | Conformis, Inc., Burlington MA, US |
| Decision | Substantially Equivalent, Sep 20, 2007 |
| Received | Aug 23, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072368
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 15, 2009 | Conformis Inc ConforMIS iUni ( Unicondylar Knee System ) Left Medial Implant Kit Product Code: M57220600010.
For cemented use only. System consists of femoral and tibial components. The femoral component is C Terminated |
HSX | None listed |
| Jul 15, 2009 | Conformis Inc ConforMIS iUni ( Unicondylar Knee System ) iUni Right Medial Implant Kit Product Code : M57220600020.
For cemented use only. System consists of femoral and tibial components. The femoral component Terminated |
HSX | None listed |
| Jul 15, 2009 | Conformis Inc ConforMIS iUni ( Unicondylar Knee System iUni Right Lateral Implant Kit Product Code: M57220600040.
For cemented use only. System consists of femoral and tibial components. The femoral component is Terminated |
HSX | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.