# K992154: Bicon-Plus Acetabular Components

- Pathway: 510(k) (Traditional)
- Applicant: Plus Orthopedics
- Decided: Apr 6, 2000 after 286 days
- Product code: LPH (Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented)
- Device class: 2
- Regulation: 21 CFR 888.3358
- 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 K883921 (1988). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K883921: Omnifit Threaded Acetabular Comp. W/Micro Coating, Osteonics Corp. (1988) Summary page 1.

## Most influential descendants
- K123598: Smith & Nephew, Inc. Hip System Instrumentation (2013), 0 descendants of its own

## Indications for use
The BICON-PLUS Acetabular Components are intended for use in primary and revision total hip arthroplasty where the acetabular socket needs restructuring.

Source page: https://510kreport.com/device/K992154
Methodology: https://510kreport.com/methodology