510(k) K071879 ยท NQP Posterior Metal/Polymer Spinal System, Fusion
ZIMMER DTO IMPLANT
| Applicant | Zimmer Spine, Inc., Minneapolis MN, US |
| Decision | Unknown, Oct 5, 2007 |
| Received | Jul 9, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071879
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Nov 6, 2012 | Zimmer, Inc. DTO" Implant Terminated |
NQP | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.