# K950761: Index Acetabulat Component

- Pathway: 510(k) (Traditional)
- Applicant: Biomet, Inc.
- Decided: May 2, 1995 after 74 days
- Product code: JDI (Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented)
- Device class: 2
- Regulation: 21 CFR 888.3350
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
481 later devices descend from it; 1 cites it directly.
0 of 482 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K023357: Arcpm 1050 Resin-Hips (2002), 480 descendants of its own
- K042051: Arcomxl Polyethylene Liners (2005), 355 descendants of its own
- K051411: Arcomxl Polyethylene Liners and Biolox Delta Heads (2005), 344 descendants of its own
- K061312: 36MM Biolox Delta Ceramic Heads (2006), 343 descendants of its own
- K050327: E-Poly (Vitamin E) Acetabular Liners (2005), 289 descendants of its own

Source page: https://510kreport.com/device/K950761
Methodology: https://510kreport.com/methodology