510(k) K061640 ยท GWM Device, Monitoring, Intracranial Pressure
INTEGRA MOBIUS MULTI-MODALITY MONITORING SYSTEM
| Applicant | Integra LifeSciences Corporation, Planisboro NJ, US |
| Decision | Substantially Equivalent, Jul 27, 2006 |
| Received | Jun 12, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061640
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.