Arrowhead Medical Device Technologies, LLC
United StatesFDA applicant, unverified
- Devices
- 2
What Arrowhead Medical Device Technologies, LLC makes
Arrowhead Medical Device Technologies, LLC develops software and instrumentation for deformity analysis and correction in orthopedic applications, including the DACS system and the ARROW-LOK DIGITAL SYSTEM for surgical planning and execution.
These products are regulated as Class II devices under FDA 510(k) clearance requirements and are listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Arrow-Lok Digital System Ref K112675
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Arrowhead Medical Device Technologies, LLC have in the registry?
The registry currently lists 2 devices for Arrowhead Medical Device Technologies, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Arrowhead Medical Device Technologies, LLC's devices?
Among its 2 most recently registered devices, Arrowhead Medical Device Technologies, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Arrowhead Medical Device Technologies, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Arrowhead Medical Device Technologies, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Arrowhead Medical Device Technologies, LLC in the registry?
The most recently registered devices listed for Arrowhead Medical Device Technologies, LLC include Deformity Analysis and Correction Software (DACS) and Instrumentation and ARROW-LOK DIGITAL SYSTEM.