New Business Development, LLC
United StatesFDA applicant, unverified
- Devices
- 4
What New Business Development, LLC makes
New Business Development, LLC manufactures spinal implants and interventional devices, including vertebral body replacements for spinal stabilization, head screws for fixation, cement restrictor devices to control bone cement flow, and disposable RF cannulae for ablation procedures.
The company’s portfolio is regulated under FDA Class II devices, with products authorised via the 510(k) pathway. These devices are listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Phenix Vertebral Body Replacement Ref K072029
Regimes: 510(k) Registry: 510(k)Nbd Head Screw Ref K050377
Regimes: 510(k) Registry: 510(k)Nbd Cement Restrictor Device Ref K021788
Regimes: 510(k) Registry: 510(k)Nbd Disposable Rf Cannulae Ref K032196
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does New Business Development, LLC have in the registry?
The registry currently lists 4 devices for New Business Development, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list New Business Development, LLC's devices?
Among its 4 most recently registered devices, New Business Development, LLC has devices listed in FDA 510(k) (4 devices).
What risk classes do New Business Development, LLC's devices fall under?
Among its 4 most recently registered devices, the classes recorded for New Business Development, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from New Business Development, LLC in the registry?
The most recently registered devices listed for New Business Development, LLC include PHENIX VERTEBRAL BODY REPLACEMENT, NBD HEAD SCREW, NBD CEMENT RESTRICTOR DEVICE and NBD DISPOSABLE RF CANNULAE.