510(k) K071905 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM (PCFS)
| Applicant | Lanx, LLC, Philadelphia PA, US |
| Decision | Substantially Equivalent, Dec 28, 2007 |
| Received | Jul 10, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071905
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.