Mcnicoll Surgical, Inc.
CanadaFDA applicant, unverified FDA FEI 3031680559
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Mcnicoll Surgical, Inc. makes
Mcnicoll Surgical, Inc. manufactures the Falco Fusion System, a surgical device designed for spinal fusion procedures, combining bone graft materials and fixation components to promote bone growth and stability in the spine.
The Falco Fusion System is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Falco Fusion System Ref K253611
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3031680559
- Address
- 702-1750 Ave de Vitre, Quebec City
Frequently asked questions
How many devices does Mcnicoll Surgical, Inc. have in the registry?
The registry currently lists 1 device for Mcnicoll Surgical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mcnicoll Surgical, Inc.'s devices?
Among its 1 most recently registered device, Mcnicoll Surgical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Mcnicoll Surgical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mcnicoll Surgical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mcnicoll Surgical, Inc. in the registry?
The most recently registered devices listed for Mcnicoll Surgical, Inc. include Falco Fusion System.