Chiral Surgical
Country not established
- Devices
- 1
What Chiral Surgical makes
Chiral Surgical manufactures the Chiral Surgical Pedicle Screw System, a spinal fixation device used for orthopedic applications in the lumbar and thoracic spine.
The company’s portfolio is regulated under FDA 510(k) clearance as a Class II medical device and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Chiral Surgical Pedicle Screw System Ref K181995
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Chiral Surgical have in the registry?
The registry currently lists 1 device for Chiral Surgical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Chiral Surgical's devices?
Among its 1 most recently registered device, Chiral Surgical has devices listed in FDA 510(k) (1 device).
What risk classes do Chiral Surgical's devices fall under?
Among its 1 most recently registered device, the classes recorded for Chiral Surgical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Chiral Surgical in the registry?
The most recently registered devices listed for Chiral Surgical include Chiral Surgical Pedicle Screw System.