International safety notice
Software StealthStation Cranial versión 3 o posterior con Licencia StealthStation DBS (Estimulación Cerebral Profunda) and Software StealthStation S8 con Licencia Stealth DBS (Estimulación Cerebral Profunda)utilizados con el sistema esterotáctico Nexframe
Spain / AEMPS · ESP · Sep 11, 2019
Key facts
| Title | Software StealthStation Cranial versión 3 o posterior con Licencia StealthStation DBS (Estimulación Cerebral Profunda) and Software StealthStation S8 con Licencia Stealth DBS (Estimulación Cerebral Profunda)utilizados con el sistema esterotáctico Nexframe |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Software StealthStation Cranial versión 3 o posterior con Licencia StealthStation DBS (Estimulación Cerebral Profunda) and Software StealthStation S8 con Licencia Stealth DBS (Estimulación Cerebral Profunda)utilizados con el sistema esterotáctico Nexframe |
| Manufacturer | Medtronic Navigation Inc., Estados Unidos. |
| Models | 916250540, 54326, 28022, 2019-490, FA884, 91.822.52.89, 28050 |
| Event type | Safety Notice |
| Date | Sep 11, 2019 |
At a glance
- No Recall
- Yes Field safety notice
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1