# K192450: Precision Casting Solutions Total Hip System

- Pathway: 510(k) (Traditional)
- Applicant: Precision Casting Solution, LLC
- Decided: Dec 17, 2019 after 102 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: 11 generations back to K810258 (1981). 76 ancestors in all.
No later device cites it as a predicate yet.
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.
- K151424: The Progressive Orthopaedic Total Hip System, The Progressive Orthopaedic Company, LLC (2016) Summary page 4.

## Indications for use
The Precision Casting Solutions Total Hip System implant components are indicated for use in cementless reconstruction of the articulating surface of femoral and/or 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/K192450
Methodology: https://510kreport.com/methodology