Permedica
Country not established
- Devices
- 1
What Permedica makes
Permedica manufactures the GKS PRIME FLEX CR TOTAL KNEE SYSTEM, a knee replacement device designed for total knee arthroplasty procedures.
The company’s portfolio is regulated under FDA Class II devices, with the GKS PRIME FLEX CR system authorised via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Gks Prime Flex Cr Total Knee System Ref K122975
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Permedica have in the registry?
The registry currently lists 1 device for Permedica. Devices recorded under merged duplicate company entries are counted once.
Which registries list Permedica's devices?
Among its 1 most recently registered device, Permedica has devices listed in FDA 510(k) (1 device).
What risk classes do Permedica's devices fall under?
Among its 1 most recently registered device, the classes recorded for Permedica's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Permedica in the registry?
The most recently registered devices listed for Permedica include GKS PRIME FLEX CR TOTAL KNEE SYSTEM.