Medtronic Tyrx, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Medtronic Tyrx, Inc. makes
Medtronic Tyrx, Inc. manufactures absorbable antibacterial envelopes designed to reduce infection risk around neurostimulation devices, such as deep brain stimulators and spinal cord stimulators.
The company’s portfolio is regulated under FDA Class II devices and authorised via the 510(k) pathway. Products are listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
TYRX Neuro Absorbable Antibacterial Envelope Ref K150291
Regimes: 510(k) Registry: 510(k)TYRX Neuro Absorbable Antibacterial Envelope Ref K142611
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medtronic Tyrx, Inc. have in the registry?
The registry currently lists 2 devices for Medtronic Tyrx, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medtronic Tyrx, Inc.'s devices?
Among its 2 most recently registered devices, Medtronic Tyrx, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Medtronic Tyrx, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Medtronic Tyrx, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medtronic Tyrx, Inc. in the registry?
The most recently registered devices listed for Medtronic Tyrx, Inc. include TYRX Neuro Absorbable Antibacterial Envelope.