Arthrex Arthroscopy Instruments, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Arthrex Arthroscopy Instruments, Inc. makes
The company manufactures arthroscopic cannulas, including the CANNULA MODEL AR-6001 and CANNULA MODEL AR-6551, designed for use in joint surgeries such as knee, shoulder, or elbow arthroscopy. These devices facilitate the delivery of instruments or irrigation fluids during minimally invasive procedures.
The portfolio consists of Class II devices, each authorised via the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Cannula Model Ar-6001 Ref K880295
Regimes: 510(k) Registry: 510(k)Cannula Model Ar-6551 Ref K881792
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Arthrex Arthroscopy Instruments, Inc. have in the registry?
The registry currently lists 2 devices for Arthrex Arthroscopy Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Arthrex Arthroscopy Instruments, Inc.'s devices?
Among its 2 most recently registered devices, Arthrex Arthroscopy Instruments, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Arthrex Arthroscopy Instruments, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Arthrex Arthroscopy Instruments, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Arthrex Arthroscopy Instruments, Inc. in the registry?
The most recently registered devices listed for Arthrex Arthroscopy Instruments, Inc. include CANNULA MODEL AR-6001 and CANNULA MODEL AR-6551.