# K001984: Progeny Forged Cocr Cemented Femoral Component

- Pathway: 510(k) (Traditional)
- Applicant: Stelkast Company
- Decided: Sep 27, 2000 after 90 days
- Product code: JDG (Prosthesis, Hip, Femoral Component, Cemented, Metal)
- Device class: 2
- Regulation: 21 CFR 888.3360
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices 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.

## Most influential descendants
- K254043: TRIVANCE™ Hip Stem (2026), 0 descendants of its own

## Indications for use
1. Joint impairment from arthritis (rheumatoid, osteo and posttraumatic). 2. Revision of Wed femoral head replacements. 3. When alternative reconstructive techniques are not viable. 4. When arthrodesis is contraindicated. 5. Avascular necrosis or fracture of the femoral head. 6. Congenital defects that will allow adequate fanctbn of the system

Source page: https://510kreport.com/device/K001984
Methodology: https://510kreport.com/methodology