# K992153: PE-Plus Acetabular Cup

- Pathway: 510(k) (Traditional)
- Applicant: Plus Orthopedics
- Decided: Sep 23, 1999 after 90 days
- Product code: JDI (Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented)
- Device class: 2
- Regulation: 21 CFR 888.3350
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K855231 (1986). 5 ancestors in all.
15 later devices descend from it; 2 cite it directly.
0 of 21 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K971705: Implex Hep Acetabular Cup System, Cemented, Implex Corp. (1997) Summary page 1.
- K972792: Duration Stabilized Uhmwpe Acetabular Components, Howmedica Corp. (1997) Summary page 1.

## Most influential descendants
- K112158: Modulus Stems, Modulus Necks, Modular Femoral Heads, Cemented Cups, Lock Bipolar Heads (2012), 13 descendants of its own
- K141327: Minima S System (2014), 5 descendants of its own
- K152903: REVIVAL (TM) Modular Revision Hip Stem (2016), 4 descendants of its own
- K140975: Mastersl Femoral Stem (2014), 4 descendants of its own
- K191374: Revival Modular Hip Stem (2019), 3 descendants of its own

## Indications for use
The PE-PLUS Acetabular Cup is intended for cemented use in hip arthroplasty where the acetabular socket needs restructuring.

Source page: https://510kreport.com/device/K992153
Methodology: https://510kreport.com/methodology