510(k) K992591 ยท GWM Device, Monitoring, Intracranial Pressure
CODMAN SINGLE AND DOUBLE LUMEN SKULL BOLT KITS
| Applicant | Codman & Shurtleff, Inc., Raynham MA, US |
| Decision | Substantially Equivalent, Oct 15, 1999 |
| Received | Aug 2, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992591
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.