# K955033: Rim Flare Acetabular Component

- Pathway: 510(k) (Traditional)
- Applicant: Intermedics Orthopedics
- Decided: Jan 31, 1996 after 90 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
No predicates in its family tree.
328 later devices descend from it; 1 cites it directly.
0 of 329 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
- K983509: Inter-OP Acetabular System - Durasul Acetabular Insert (1999), 327 descendants of its own
- K993259: Inter-OP Durasul Acetabular Inserts/Cocr Femoral Heads (2000), 326 descendants of its own
- K022902: Smith & Nephew Hip System (2002), 285 descendants of its own
- K040191: Bicontact Hip Stem and Femoral Head (2004), 267 descendants of its own
- K042344: Excia Total Hip System (2005), 198 descendants of its own

Source page: https://510kreport.com/device/K955033
Methodology: https://510kreport.com/methodology