# K001078: Sulzer Orthopedics MS-30 Femoral Stem

- Pathway: 510(k) (Traditional)
- Applicant: Sulzer Orthopedics, Inc.
- Decided: Jun 23, 2000 after 80 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.
9 later devices descend from it; 1 cites it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K040803: MS-30 Femoral Stem Standard and Lateral (2004), 8 descendants of its own
- K133370: Remedy Hip Stem, Pegasus Hip Stem, Evolve Helios Hip Stem, Evolve Masters Hip Stem, Evolve Distal Centralizer, Evolve CE (2014), 5 descendants of its own
- K143184: Evolve UniPolar Head (2015), 1 descendant of its own
- K131884: Avenir Cemented Hip Stem (2013), 1 descendant of its own
- K243043: Origin™ Cemented Hip Stem (2025), 0 descendants of its own

Source page: https://510kreport.com/device/K001078
Methodology: https://510kreport.com/methodology