Intellirod Spine, Inc.
Country not established
- Devices
- 1
What Intellirod Spine, Inc. makes
Intellirod Spine, Inc. manufactures the LOADPRO™ Intraoperative Rod Strain Sensor, a device designed to measure rod strain during spinal surgery to assess implant integrity and alignment in real time.
The LOADPRO™ Intraoperative Rod Strain Sensor is classified as a Class II medical device and is authorised via the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
LOADPRO™ Intraoperative Rod Strain Sensor Ref DEN180012
Regimes: De Novo Registry: De Novo
Frequently asked questions
How many devices does Intellirod Spine, Inc. have in the registry?
The registry currently lists 1 device for Intellirod Spine, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Intellirod Spine, Inc.'s devices?
Among its 1 most recently registered device, Intellirod Spine, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Intellirod Spine, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Intellirod Spine, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Intellirod Spine, Inc. in the registry?
The most recently registered devices listed for Intellirod Spine, Inc. include LOADPRO™ Intraoperative Rod Strain Sensor.