510(k) K033395 ยท GXO Strip, Craniosynostosis, Preformed
CODMAN DURAL GRAFT IMPLANT, MODELS 80-1471, 80-1472, 80-1473, 80-1474, 80-1475, 80-1476, 80-1477, 80-1478, 80-1480, 80-1
| Applicant | Codman & Shurtleff, Inc., Raynham MA, US |
| Decision | Substantially Equivalent, Feb 25, 2004 |
| Received | Oct 23, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K033395
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.