NQP

Posterior Metal/Polymer Spinal System, Fusion

Product code

NQP

Device name

Posterior Metal/Polymer Spinal System, Fusion

Device class

Class 2

21 CFR

21 CFR 888.3070

Medical specialty

Orthopedic

Marketing pathway

510(K)

Flag

Implant

510(k) clearances (all years, FDA)

22 (all years; only the last 3 years are listed here)

FDA classification definition

This device is a posterior spinal system that contains polymer and metal components. This spinal system is to be used with bone graft and is an adjunct to fusion in the treatment of acute and chronic instabilities or deformities of the thoracic, lumbar, and sacral spine.

Definition text from the FDA device classification database (U.S. federal government work, public domain).