510(k) K031702 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
REFLEX ANTERIOR CERVICAL PLATE SYSTEM
| Applicant | Howmedica Osteonics, Allendale NJ, US |
| Decision | Substantially Equivalent, Aug 8, 2003 |
| Received | Jun 2, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K031702
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.