510(k) K041518 ยท GXQ Dura Substitute
CODMAN DURAFORM DURAL GRAFT IMPLANT
| Applicant | Codman & Shurtleff, Inc., Raynham MA, US |
| Decision | Substantially Equivalent, Jun 22, 2004 |
| Received | Jun 7, 2004 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K041518
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.