510(k) K121159 ยท GWM Device, Monitoring, Intracranial Pressure
INTEGRA CAMINO FLEX VENTRICULAR INTRACRANIAL PRESSURE MONITORING KIT WITH INTRGRA CAMINO FLEX ADAPTER
| Applicant | Integra Lifescience Corportation, Planisboro NJ, US |
| Decision | Substantially Equivalent, Jul 20, 2012 |
| Received | Apr 16, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K121159
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.