# K022382: RHS Acetabular Component

- Pathway: 510(k) (Traditional)
- Applicant: Signal Medical Corp.
- Decided: Oct 4, 2002 after 74 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
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Indications for use
OSTEOARTHRITIS RHEUMATOID ARTHRITIS TRAUMATIC ARTHRITIS WHERE THE USE OF A MORE CONSERVATIVE PROCEDURE HAS FAILED OR IS UNACCEPTABLE INTENDED FOR NON-CEMENTED USE SINGLE USE ONLY

Source page: https://510kreport.com/device/K022382
Methodology: https://510kreport.com/methodology