# K030501: X-Series Integral Lateralized Hip Components

- Pathway: 510(k) (Special)
- Applicant: Biomet, Inc.
- Decided: Mar 20, 2003 after 29 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: 2 generations back to K921225 (1994). 2 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K984296: Lateralized Intergral Porous Primary Femoral Component, Biomet, Inc. (1999) Summary page 1.

## Most influential descendants
- K042029: X-Series Integral RPP Femoral Components (2004), 0 descendants of its own

## Indications for use
Non-cemented total joint replacement in cases of: Noninflamatory degenerative joint disease including osteoarthritis and avascular necrosis Rheumatoid arthritis Correction of functional deformity Treatment of non-union, femoral neck fracture, and trochanteric fractures of the proximal femur with head involvement, unmanageable by other techniques. Revision of previously failed total hip arthroplasty

Source page: https://510kreport.com/device/K030501
Methodology: https://510kreport.com/methodology