# K923452: Pmi Hip Femoral

- Pathway: 510(k) (Traditional)
- Applicant: Biomet, Inc.
- Decided: Feb 16, 1994 after 582 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.
3 later devices descend from it; 2 cite it directly.
0 of 4 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
- K053246: Patient Matched Hip Stem (2006), 1 descendant of its own
- K123598: Smith & Nephew, Inc. Hip System Instrumentation (2013), 0 descendants of its own
- K030048: HA Pmi Femoral Hip Stem (2003), 0 descendants of its own

Source page: https://510kreport.com/device/K923452
Methodology: https://510kreport.com/methodology