# K151424: The Progressive Orthopaedic Total Hip System

- Pathway: 510(k) (Traditional)
- Applicant: The Progressive Orthopaedic Company, LLC
- Decided: Jul 27, 2016 after 426 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: 10 generations back to K810258 (1981). 75 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 77 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K143314: Progressive Orthopaedic Total Hip System, The Progressive Orthopaedic Company, LLC (2015) Summary page 4.
- K140701: Novohip Bipolar Head/Novohip Vitamin E Liner/ Bone Screws/ Hole Plug, Novosource, Inc. (2014) Summary page 4.

## Most influential descendants
- K192450: Precision Casting Solutions Total Hip System (2019), 0 descendants of its own

## Indications for use
The Progressive Orthopaedic Total Hip System implant components are indicated for use in cementless reconstruction of the articulating surface of femoral and acetabular portions of the hip that are severely disabled and/or very painful as a result of: • Non-inflammatory degenerative joint disease including osteoarthritis and avascular necrosis • Rheumatoid arthritis or traumatic arthritis • Correction of functional deformity • Non-union femoral neck fracture • Trochanteric fractures of the proximal femur with head involvement which is unmanageable using other techniques. The components can be used for primary hip arthroplasty or for revision of a failed total hip arthroplasty.

Source page: https://510kreport.com/device/K151424
Methodology: https://510kreport.com/methodology