510(k) K092695 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
TRANSCORP TRANS-PLATE ANTERIOR CERVICAL PLATE SYSTEM
| Applicant | Transcorp, Inc., Byron Center MI, US |
| Decision | Substantially Equivalent, May 21, 2010 |
| Received | Sep 2, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092695
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.