Innovative Spinal Technologies, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Innovative Spinal Technologies, Inc. makes
Innovative Spinal Technologies, Inc. manufactures spinal fixation and fusion devices, including anterior cervical plates, intervertebral body fusion implants, vertebral body replacement systems, and pedicle screw systems for surgical stabilization of the spine.
These products are classified as Class II medical devices in the US and are listed under the FDA’s 510(k) clearance pathway. The company is based in the United States.
Catalogue
Ist Anterior Cervical Plate System Ref K072650
Regimes: 510(k) Registry: 510(k)Paramount Intervertebral Body Fusion Device Ref K072120
Regimes: 510(k) Registry: 510(k)Paramount Vbr System Ref K062759
Regimes: 510(k) Registry: 510(k)Ist Pedicle Screw System Ref K053276
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Innovative Spinal Technologies, Inc. have in the registry?
The registry currently lists 4 devices for Innovative Spinal Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Innovative Spinal Technologies, Inc.'s devices?
Among its 4 most recently registered devices, Innovative Spinal Technologies, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Innovative Spinal Technologies, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Innovative Spinal Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Innovative Spinal Technologies, Inc. in the registry?
The most recently registered devices listed for Innovative Spinal Technologies, Inc. include IST ANTERIOR CERVICAL PLATE SYSTEM, PARAMOUNT INTERVERTEBRAL BODY FUSION DEVICE, PARAMOUNT VBR SYSTEM and IST PEDICLE SCREW SYSTEM.