510(k) K802137 ยท GWM Device, Monitoring, Intracranial Pressure
CHEEK EPIDURAL SCREW
| Applicant | Codman & Shurtleff, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 31, 1980 |
| Received | Sep 4, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802137
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.