Tides Medical
Country not established
- Devices
- 1
What Tides Medical makes
Tides Medical manufactures the Bluefin Interbody System, a spinal interbody fusion device designed for anterior lumbar interbody fusion (ALIF) procedures. The system includes cages and instrumentation tailored for minimally invasive spinal surgeries, providing structural support and promoting bone fusion in the lumbar spine.
The Bluefin Interbody System is classified as a Class II medical device in the US and has undergone 510(k) clearance through the FDA regulatory pathway. The company is based in the United States.
Catalogue
Bluefin Interbody System Ref K143479
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tides Medical have in the registry?
The registry currently lists 1 device for Tides Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tides Medical's devices?
Among its 1 most recently registered device, Tides Medical has devices listed in FDA 510(k) (1 device).
What risk classes do Tides Medical's devices fall under?
Among its 1 most recently registered device, the classes recorded for Tides Medical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tides Medical in the registry?
The most recently registered devices listed for Tides Medical include Bluefin Interbody System.