510(k) K050082 ยท NQW Orthosis, Spine, Plate, Laminoplasty, Metal
CENTERPIECE PLATE FIXATION SYSTEM
| Applicant | Medtronic Sofamor Danek, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, Jun 6, 2005 |
| Received | Jan 13, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K050082
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.