510(k) K133754 ยท GWM Device, Monitoring, Intracranial Pressure
INTEGRA CAMINO FLEX VENTRICULAR INTRACRANIAL PRESSURE MONITORING KIT WITH FLEX ADAPTER
| Applicant | Integra LifeSciences Corporation, Plainsboro NJ, US |
| Decision | Substantially Equivalent, Mar 6, 2014 |
| Received | Dec 9, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133754
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.