Meditech Advisors, LLC
United StatesFDA applicant, unverified
- Devices
- 2
What Meditech Advisors, LLC makes
Meditech Advisors, LLC manufactures intervertebral body fusion devices, including the TALOS and TALOS-C systems designed for spinal fusion procedures in both lumbar and cervical regions.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Talos Intervertebral Body Fusion Device Ref K090707
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Meditech Advisors, LLC have in the registry?
The registry currently lists 2 devices for Meditech Advisors, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Meditech Advisors, LLC's devices?
Among its 2 most recently registered devices, Meditech Advisors, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Meditech Advisors, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Meditech Advisors, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Meditech Advisors, LLC in the registry?
The most recently registered devices listed for Meditech Advisors, LLC include TALOS INTERVERTEBRAL BODY FUSION DEVICE and TALOS-C CERVICAL INTERVERTEBRAL BODY FUSION DEVICES.