Sigmedics, Inc.
Country not established
- Devices
- 1
What Sigmedics, Inc. makes
Sigmedics, Inc. manufactures the PARASTEP-I, a medical device designed for the treatment of spinal conditions, specifically intended for spinal fusion procedures.
The PARASTEP-I is classified as a Class III device under FDA regulations and is listed under the Premarket Approval (PMA) pathway. The company is based in the United States.
Catalogue
Parastep-I Ref P900038
Regimes: PMA Registry: PMA
Frequently asked questions
How many devices does Sigmedics, Inc. have in the registry?
The registry currently lists 1 device for Sigmedics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sigmedics, Inc.'s devices?
Among its 1 most recently registered device, Sigmedics, Inc. has devices listed in FDA PMA (1 device).
What risk classes do Sigmedics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sigmedics, Inc.'s devices are Class III. Each device page shows its own class and authorisation.
What are the newest devices from Sigmedics, Inc. in the registry?
The most recently registered devices listed for Sigmedics, Inc. include PARASTEP-I.