# K071053: Recap HA Press-Fit Femoral Resurfacing Head

- Pathway: 510(k) (Special)
- Applicant: Biomet, Inc.
- Decided: Jun 29, 2007 after 77 days
- Product code: KXA (Prosthesis, Hip, Femoral, Resurfacing)
- Device class: 2
- Regulation: 21 CFR 888.3400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K983452 (1998). 4 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K023188: Press-Fit Head Resurfacing Device, Biomet Orthopedics, Inc. (2002) Summary page 1.

## Most influential descendants
- K092198: Cormet Cementless Resurfacing Femoral Head (2010), 0 descendants of its own

## Indications for use
Non-inflammatory degenerative joint disease, including osteoarthritis and avascular necrosis, and rheumatoid arthritis. The device is a single use implant intended for press-fit application.

Source page: https://510kreport.com/device/K071053
Methodology: https://510kreport.com/methodology