Portland Orthopaedics Limited
Country not established
- Devices
- 1
What Portland Orthopaedics Limited makes
Portland Orthopaedics Limited manufactures orthopaedic implants, including cobalt-chrome femoral heads used in hip replacements. These components are designed for joint arthroplasty procedures to restore mobility and function in patients with degenerative joint conditions.
The company’s portfolio is regulated under FDA’s Class II device classification, requiring 510(k) clearance. The femoral head implant is listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Portland Cobalt Chrome Femoral Head Ref K063278
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Portland Orthopaedics Limited have in the registry?
The registry currently lists 1 device for Portland Orthopaedics Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Portland Orthopaedics Limited's devices?
Among its 1 most recently registered device, Portland Orthopaedics Limited has devices listed in FDA 510(k) (1 device).
What risk classes do Portland Orthopaedics Limited's devices fall under?
Among its 1 most recently registered device, the classes recorded for Portland Orthopaedics Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Portland Orthopaedics Limited in the registry?
The most recently registered devices listed for Portland Orthopaedics Limited include PORTLAND COBALT CHROME FEMORAL HEAD.