J.B.S. (Usa), Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
Catalogue
J.B.S. T.T.A Screw Ref K955710
510(k) 510(k)J.B.S. Anterior Spine System(R) Ref K950209
510(k) 510(k)
Frequently asked questions
How many devices does J.B.S. (Usa), Inc. have in the registry?
The registry currently lists 2 devices for J.B.S. (Usa), Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list J.B.S. (Usa), Inc.'s devices?
Among its 2 most recently registered devices, J.B.S. (Usa), Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do J.B.S. (Usa), Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for J.B.S. (Usa), Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from J.B.S. (Usa), Inc. in the registry?
The most recently registered devices listed for J.B.S. (Usa), Inc. include J.B.S. T.T.A SCREW and J.B.S. ANTERIOR SPINE SYSTEM(R).