Figure 8 Surgical, Incorporated
Country not established
- Devices
- 1
What Figure 8 Surgical, Incorporated makes
Figure 8 Surgical, Incorporated manufactures the Figure 8 Sternotomy Closure Device, a system designed for reapproximating sternal edges after median sternotomy procedures.
The device is classified as Class II under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Figure 8 Sternotomy Closure Device Ref K110541
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Figure 8 Surgical, Incorporated have in the registry?
The registry currently lists 1 device for Figure 8 Surgical, Incorporated. Devices recorded under merged duplicate company entries are counted once.
Which registries list Figure 8 Surgical, Incorporated's devices?
Among its 1 most recently registered device, Figure 8 Surgical, Incorporated has devices listed in FDA 510(k) (1 device).
What risk classes do Figure 8 Surgical, Incorporated's devices fall under?
Among its 1 most recently registered device, the classes recorded for Figure 8 Surgical, Incorporated's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Figure 8 Surgical, Incorporated in the registry?
The most recently registered devices listed for Figure 8 Surgical, Incorporated include FIGURE 8 STERNOTOMY CLOSURE DEVICE.