# K030867: Eska Modular Hip System Cemented

- Pathway: 510(k) (Traditional)
- Applicant: Eska Implants GmbH
- Decided: Sep 22, 2003 after 187 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. The FDA summary names its predicate without a number.
- (no number) Omnifit Hip System (Osteonics): named in the summary without a submission number
- (no number) PFC Cemented Total Hip System (Johnson & Johnson): named in the summary without a submission number
- (no number) Link SPII Hip System (Link): named in the summary without a submission number
- (no number) Exactech Cemented Total Hip System (Exactech): named in the summary without a submission number

## Indications for use
The ESKA Modular Hip System Cemented is indicated for cemented use in the treatment of sevcrcly disabled hip joints resulting from painful osteo-, rheumatoid and post-traumatic arthritis. and the late stages of avascular necrosis, and for revision of previous hip surgeries.

Source page: https://510kreport.com/device/K030867
Methodology: https://510kreport.com/methodology