Acro Composites, LLC
Country not established
- Devices
- 1
What Acro Composites, LLC makes
Acro Composites, LLC manufactures spinal interbody devices designed for intervertebral fusion procedures, including the Acro Composites Interbody System. These products are intended for use in the lumbar and cervical spine to restore disc height and promote structural stability during surgical interventions.
The company’s portfolio is regulated under FDA Class II devices, with product authorisations obtained through the 510(k) clearance pathway. The devices are listed in the FDA’s 510(k) database and comply with applicable US medical device regulations.
Catalogue
Acro Composites Interbody System Ref K230478
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Acro Composites, LLC have in the registry?
The registry currently lists 1 device for Acro Composites, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Acro Composites, LLC's devices?
Among its 1 most recently registered device, Acro Composites, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Acro Composites, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Acro Composites, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Acro Composites, LLC in the registry?
The most recently registered devices listed for Acro Composites, LLC include Acro Composites Interbody System.