International safety notice
Extensión percutánea del Sistema de neuroestimulación implantable InterStim™, modelo 3560030 y 3560022.
Spain / AEMPS · ESP · Oct 26, 2020
Key facts
| Title | Extensión percutánea del Sistema de neuroestimulación implantable InterStim™, modelo 3560030 y 3560022. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Extensión percutánea del Sistema de neuroestimulación implantable InterStim™, modelo 3560030 y 3560022. |
| Manufacturer | Medtronic, Inc, EEUU. |
| Models | 28022, 978B1, FA933, 3560030, 353101, 63036, VERIFY353101, 2020-603, 91.822.52.89, 3560022, 978A1, 28050 |
| Event type | Safety Notice |
| Date | Oct 26, 2020 |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 Matching device models in FDA data
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