510(k) K091253 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
THORACOLUMBAR PLATE, MODEL 1208-41FXX, LUMBER PLATE, MODEL 1208-41FXXL, SACRAL PLATE, MODEL 1208-41FXXS
| Applicant | K2m, Inc., Leesburg VA, US |
| Decision | Substantially Equivalent, Jun 4, 2009 |
| Received | Apr 29, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K091253
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.