Pipeline Biotechnology
Country not established
- Devices
- 1
What Pipeline Biotechnology makes
Pipeline Biotechnology manufactures the Pipeline Total Hip System, a line extension for total hip arthroplasty, designed to replace damaged or diseased hip joints with prosthetic components.
The Pipeline Total Hip System is classified as a Class II medical device in the US and is authorised through the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Pipeline Total Hip System (Line Extension) Ref K132626
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pipeline Biotechnology have in the registry?
The registry currently lists 1 device for Pipeline Biotechnology. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pipeline Biotechnology's devices?
Among its 1 most recently registered device, Pipeline Biotechnology has devices listed in FDA 510(k) (1 device).
What risk classes do Pipeline Biotechnology's devices fall under?
Among its 1 most recently registered device, the classes recorded for Pipeline Biotechnology's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pipeline Biotechnology in the registry?
The most recently registered devices listed for Pipeline Biotechnology include PIPELINE TOTAL HIP SYSTEM (LINE EXTENSION).