Altus Partners
United Statesfrom the FDA registration address FDA FEI 3009049161
- Devices
- 18
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Altus Partners makes
Altus Partners makes medical devices such as the ALTUS SPINE PEDICLE SCREW SYSTEM, which is a type of spinal implant.
The company's portfolio is regulated as Class II devices and is listed in the FDA 510(k) registry, with the company based in the US.
Catalogue
Search and filter all 18 devicesCompany details
- FDA FEI number
- 3009049161
- Address
- 1340 ENTERPRISE DR, WEST CHESTER, PA, 19380
Frequently asked questions
How many devices does Altus Partners have in the registry?
The registry currently lists 18 devices for Altus Partners. Devices recorded under merged duplicate company entries are counted once.
Which registries list Altus Partners's devices?
Among its 18 most recently registered devices, Altus Partners has devices listed in FDA 510(k) (18 devices).
What risk classes do Altus Partners's devices fall under?
Among its 18 most recently registered devices, the classes recorded for Altus Partners's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Altus Partners in the registry?
The most recently registered devices listed for Altus Partners include Altus Spine Titanium Interbody Fusion System, Altus Spine Pedicle Screw System, Altus Spine Interbody Fusion System and Altus Spine Interbody Standalone Fusion System.