# Shoulder Prosthesis, Reverse Configuration
> **Product code: PHX** · Class II — Moderate Risk (510(k) clearance required) · Orthopedic · 21 CFR 888.3660
## Classification
- **FDA Product Code:** PHX
- **Device class:** Class II — Moderate Risk (510(k) clearance required)
- **Regulation:** 21 CFR 888.3660
- **Review panel:** OR
- **Medical specialty:** Orthopedic
- **Submission type:** 1
- **GMP exempt:** N
- **Life sustaining:** N
- **Implant:** Y
- **Third-party review:** N
## Definition

Intended to be used to relieve pain and to replace the glenoid and humeral side of the shoulder joint in order to restore mobility in a grossly rotator cuff deficient joint with severe arthropathy or a previous joint replacement with a grossly rotator cuff deficient joint.

## Market data
- **Cleared 510(k) submissions:** 200
- **Registered establishments:** 191
## Source
- [FDA Device Classification](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpcd/classification.cfm?ID=PHX)
---
*AI Analytics · CC0 1.0*