Medtronic Percusurge, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Medtronic Percusurge, Inc. makes
Medtronic Percusurge, Inc. manufactures temporary occlusion and aspiration systems designed for intravascular use, including the Percusurge GuardWire Plus and its modified versions. These devices are intended for percutaneous coronary interventions, particularly for removing thrombus or debris during procedures like atherectomy or stent placement.
The company’s products are classified as Class II devices under FDA regulations and are authorised via the 510(k) pathway. The portfolio is listed in the FDA’s 510(k) database, and the manufacturer 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 Medtronic Percusurge, Inc. have in the registry?
The registry currently lists 2 devices for Medtronic Percusurge, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medtronic Percusurge, Inc.'s devices?
Among its 2 most recently registered devices, Medtronic Percusurge, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Medtronic Percusurge, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Medtronic Percusurge, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medtronic Percusurge, Inc. in the registry?
The most recently registered devices listed for Medtronic Percusurge, Inc. include PERCUSURGE GUARDWIRE PLUS TEMPORARY OCCLUSION AND ASPIRATION SYSTEM and MODIFICATION TO GUARDWIRE PLUS TEMPORARY OCCLUSION & ASPIRATION SYSTEM.