# K022463: HA Modular Reach Proximal Porous and HA Modular Reach Collared Proximal Porous Femoral Stems

- Pathway: 510(k) (Special)
- Applicant: Biomet Orthopedics, Inc.
- Decided: Aug 16, 2002 after 21 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 K921274 (1994). 2 ancestors in all.
42 later devices descend from it; 2 cite it directly.
0 of 45 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K994038: Modular Reach Hip, Biomet, Inc. (1999) Summary page 1.

## Most influential descendants
- K031693: Mallory/Head  Modular Calcar with and Without HA (2003), 39 descendants of its own
- K042774: Mallory-Head Modular Calcar Stems with Interlocking Slots (2005), 38 descendants of its own
- K090757: Biomet Modular Femoral Revision System (2009), 37 descendants of its own
- K092331: Djo Surgical Revision Femoral Hip System, Model 428-14/24-140/200; 428-00-050/110; (2010), 27 descendants of its own
- K112158: Modulus Stems, Modulus Necks, Modular Femoral Heads, Cemented Cups, Lock Bipolar Heads (2012), 13 descendants of its own

## Indications for use
The indications for the HA Modular ReachTMProximal Porous and HA Modular ReachTM Collared Proximal Porous Femoral Stems are for ) Non-inflammatory degenerative joint disease including osteoarthritis and avascular necrosis; 2) Rheumatoid arthritis; 3) Correction of functional deformity; 4) Treatment of non-union, femoral neck fracture, and trochanteric fractures of the proximal femur with head involvement, unmanageable using other techniques; and 5 ) Revision procedures where other treatments or devices have failed.

Source page: https://510kreport.com/device/K022463
Methodology: https://510kreport.com/methodology