# K993713: Rim-Fix, Acetabular Cup

- Pathway: 510(k) (Traditional)
- Applicant: Surgical Implants, Inc.
- Decided: Jan 28, 2000 after 86 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
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. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The Rim-Fix, acetabular cup system is intended to be used as the pelvic component of a total hip arthroplasty. It can be implanted either as a press fit cup or cemented into the cavity. The acetabular cup is used to restore the acetabular cavity in a total joint arthroplasty and is used in conjunction with a metal femoral hip stem. The indications for use of the Rim-Fix cup system are as follows: Osteoarthritis, rheumatoid arthritis, post-traumatic arthritis or arthritis secondary to a variety of diseases or anomalies, or revision from a failed arthroplasty.

Source page: https://510kreport.com/device/K993713
Methodology: https://510kreport.com/methodology