# K053557: Eska-Libur Hip Stem

- Pathway: 510(k) (Special)
- Applicant: Eska Implants GmbH & Co.
- Decided: Jan 20, 2006 after 30 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 K993027 (2000). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K993027: Eska Modular Hip System, Specs USA, Inc. (2000) Summary page 1.

## Indications for use
The ESKA-LIBUR Hip Stem is indicated for use in the treatment rheumatoid arthritis, osteoarthritis, post-traumatic arthritis, vascular necrosis, non-union of femoral neck fractures, fracture dislocation of the hip, conversion of unsuccessful arthodeses and revision of previous hip surgeries.

Source page: https://510kreport.com/device/K053557
Methodology: https://510kreport.com/methodology