Ouroboros Medical, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 3
What Ouroboros Medical, Inc. makes
Ouroboros Medical, Inc. manufactures the XCage™ Interbody Fusion System, a spinal implant designed for interbody fusion procedures in the lumbar and thoracic spine.
The XCage™ Interbody Fusion System is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Xcage Interbody Fusion System Ref K133514
510(k) 510(k)Xtool Ref K122861
510(k) 510(k)XCage™ Interbody Fusion System Ref K160076
510(k) 510(k)
Frequently asked questions
How many devices does Ouroboros Medical, Inc. have in the registry?
The registry currently lists 3 devices for Ouroboros Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ouroboros Medical, Inc.'s devices?
Among its 3 most recently registered devices, Ouroboros Medical, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Ouroboros Medical, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Ouroboros Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ouroboros Medical, Inc. in the registry?
The most recently registered devices listed for Ouroboros Medical, Inc. include XCAGE INTERBODY FUSION SYSTEM, XTOOL and XCage™ Interbody Fusion System.