510(k) K063544 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
MODIFICATION TO PYRENEES CERVICAL PLATE SYSTEM
| Applicant | K2m, Inc., Leesburg VA, US |
| Decision | Substantially Equivalent, Feb 14, 2007 |
| Received | Nov 24, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K063544
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.