# K130550: RSP Modular Glenoid Baseplate, Glenoid Taper Adapter, Retaining Screw

- Pathway: 510(k) (Traditional)
- Applicant: Encore Medical L.P.
- Decided: Mar 24, 2014 after 385 days
- Product code: PHX (Shoulder Prosthesis, Reverse Configuration)
- Device class: 2
- Regulation: 21 CFR 888.3660
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K041066 (2005). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K041066: Encore Reverse Shoulder Prosthesis, Encore Medical L.P. (2005) Summary page 4.
- K080402: Encore Shoulder Primary Humeral Stem, Model 500-00, Encore Shoulder Humeral Head, Model 520-38, Encore Medical L.P. (2008) Summary page 4.

## Indications for use
Indicated for usc in patients with a grossly rotator cuff deficient shoulder joint with scvere arthropathy or a previously failed joint replacement with a grossly rotator cuff deficient shoulder joint. The paticnt’s joint must be anatomically and structurally suited to receive the selected implani(s), and a functional deltoid muscle is necessury to usc the device. The glenoid baseplate is intended for ccmentless application with the addition of screws for fixation. The humeral stem is intended for cemented use only.

Source page: https://510kreport.com/device/K130550
Methodology: https://510kreport.com/methodology