510(k) K081380 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
THORACOLUMBAR, LUMBAR AND SACRAL PLATES AND 6.0 AND 7.0 MM BONE SCREWS
| Applicant | K2m, Inc., Leesburg VA, US |
| Decision | Substantially Equivalent, Nov 19, 2008 |
| Received | May 16, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081380
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.