St. Jude Medical Neuromodulation
Country not established
- Devices
- 2
What St. Jude Medical Neuromodulation makes
The company designs and manufactures percutaneous neuromodulation leads and associated insertion tools, including the MTS System with wide-space quadrode leads, as well as epidural needle and stylet systems like Octrodex, Quadrodex, and Introdex.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does St. Jude Medical Neuromodulation have in the registry?
The registry currently lists 2 devices for St. Jude Medical Neuromodulation. Devices recorded under merged duplicate company entries are counted once.
Which registries list St. Jude Medical Neuromodulation's devices?
Among its 2 most recently registered devices, St. Jude Medical Neuromodulation has devices listed in FDA 510(k) (2 devices).
What risk classes do St. Jude Medical Neuromodulation's devices fall under?
Among its 2 most recently registered devices, the classes recorded for St. Jude Medical Neuromodulation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from St. Jude Medical Neuromodulation in the registry?
The most recently registered devices listed for St. Jude Medical Neuromodulation include MTS SYSTEM, WIDE-SPACE QUATTRODE PERCUTANEOUS LEADS and OCTRODEX(TM), QUATTRODEX(TM), INTRODEX(TM), EPIDURAL NEEDLE, STYLETS.