Aaxter Co., Ltd.
TaiwanFDA applicant, unverified
- Devices
- 1
What Aaxter Co., Ltd. makes
Aaxter Co., Ltd. manufactures the AAXTER A3 Posterior Spinal System, a device designed for spinal fixation and stabilization procedures in the posterior region of the spine.
The AAXTER A3 Posterior Spinal System is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Aaxter A3 Posterior Spinal System Ref K101374
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Aaxter Co., Ltd. have in the registry?
The registry currently lists 1 device for Aaxter Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aaxter Co., Ltd.'s devices?
Among its 1 most recently registered device, Aaxter Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Aaxter Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Aaxter Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Aaxter Co., Ltd. in the registry?
The most recently registered devices listed for Aaxter Co., Ltd. include AAXTER A3 POSTERIOR SPINAL SYSTEM.