510(k) K883115 ยท GWM Device, Monitoring, Intracranial Pressure
PMT SUBARACHNOID SCREW, MODEL NO.1350-2
| Applicant | Pmt Corp., Chanhassen MN, US |
| Decision | Substantially Equivalent, Aug 29, 1988 |
| Received | Jul 25, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883115
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.