Simparo, Inc.
Country not established
- Devices
- 1
What Simparo, Inc. makes
Simparo, Inc. manufactures the Simparo Anchor Line Fixation System, a medical device designed for orthopedic applications to secure surgical implants or fixation devices within bone structures.
The company’s portfolio is regulated under FDA Class II devices, with the Simparo Anchor Line Fixation System authorised via the 510(k) pathway. The device is listed in the FDA’s 510(k) database. Simparo, Inc. is based in the United States.
Catalogue
Simparo Anchor Line Fixation System Ref K222574
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Simparo, Inc. have in the registry?
The registry currently lists 1 device for Simparo, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Simparo, Inc.'s devices?
Among its 1 most recently registered device, Simparo, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Simparo, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Simparo, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Simparo, Inc. in the registry?
The most recently registered devices listed for Simparo, Inc. include Simparo Anchor Line Fixation System.