Meridian Medical
Country not established
Part of Meridian Medical Oy
- Devices
- 1
What Meridian Medical makes
Meridian Medical designs and manufactures devices for progressive tibial alignment, including tools and systems used in orthopedic procedures to correct lower limb alignment.
The company’s portfolio is regulated under FDA Class II devices, with products authorised via the 510(k) pathway. These devices are listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Pta (Progressive Tibial Alignment) Ref K060403
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Meridian Medical have in the registry?
The registry currently lists 1 device for Meridian Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Meridian Medical's devices?
Among its 1 most recently registered device, Meridian Medical has devices listed in FDA 510(k) (1 device).
What risk classes do Meridian Medical's devices fall under?
Among its 1 most recently registered device, the classes recorded for Meridian Medical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Meridian Medical in the registry?
The most recently registered devices listed for Meridian Medical include PTA (PROGRESSIVE TIBIAL ALIGNMENT).