Ignite Orthomotion
Country not established
- Devices
- 2
What Ignite Orthomotion makes
Ignite Orthomotion manufactures partial knee replacement systems, including femoral components made from porous-coated cobalt-chromium-molybdenum (CoCrMo) alloys and complete partial knee implants.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
ACHIEVE Partial Knee System Ref K242307
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ignite Orthomotion have in the registry?
The registry currently lists 2 devices for Ignite Orthomotion. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ignite Orthomotion's devices?
Among its 2 most recently registered devices, Ignite Orthomotion has devices listed in FDA 510(k) (2 devices).
What risk classes do Ignite Orthomotion's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ignite Orthomotion's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ignite Orthomotion in the registry?
The most recently registered devices listed for Ignite Orthomotion include Achieve Partial Knee System - Porous Coated CoCrMo Femoral Component and ACHIEVE Partial Knee System.