# K913060: Natural Porous Hip System

- Pathway: 510(k) (Traditional)
- Applicant: Intermedics Orthopedics
- Decided: Oct 11, 1991 after 93 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.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.
- (no number) Biolox ball manufactured by Feldmuhle Aktiengesellschaft: named in the summary without a submission number
- (no number) porous coated Ti-6Al-4V stem: named in the summary without a submission number

## Most influential descendants
- K963266: Natural Hip System Porous Stem - Collarless, Collared (1996), 0 descendants of its own

Source page: https://510kreport.com/device/K913060
Methodology: https://510kreport.com/methodology