# Posterior Metal/Polymer Spinal System, Fusion
> **Product code: NQP** · Class II — Moderate Risk (510(k) clearance required) · Orthopedic · 21 CFR 888.3070
## Classification
- **FDA Product Code:** NQP
- **Device class:** Class II — Moderate Risk (510(k) clearance required)
- **Regulation:** 21 CFR 888.3070
- **Review panel:** OR
- **Medical specialty:** Orthopedic
- **Submission type:** 1
- **GMP exempt:** N
- **Life sustaining:** N
- **Implant:** Y
- **Third-party review:** N
## 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.

## Market data
- **Cleared 510(k) submissions:** 22
- **Registered establishments:** 43
## Source
- [FDA Device Classification](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpcd/classification.cfm?ID=NQP)
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