# K113107: Msa Hip System

- Pathway: 510(k) (Special)
- Applicant: Global Manufacturing Technology
- Decided: Dec 15, 2011 after 56 days
- Product code: MEH (Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate)
- Device class: 2
- Regulation: 21 CFR 888.3353
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 12 generations back to K941847 (1994). 121 ancestors in all.
No later device cites it as a predicate yet.
1 of 121 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K102172: Msa Hip System, Global Manufacturing Technology (2011) Summary page 2.

## Indications for use
The MSA Hip System is indicated for cementless use and is intended to replace a hip joint. The device is intended for: * skeletally mature individuals undergoing primary surgery for total hip replacement * patients suffering from severe hip pain and disability due to rheumatoid arthritis, osteoarthritis, traumatic arthritis, polyarthritis, collagen disorders, avascular necrosis of the femoral head and nonunion of previous fracture of the femur. * patients with congenital hip dysplasia, protrusio acetabuli, or slipped capital femoral epiphysis * patients suffering from disability due to previous fusion * patients with acute femoral neck fractures

Source page: https://510kreport.com/device/K113107
Methodology: https://510kreport.com/methodology