# K932755: Reflection Acetabular Component

- Pathway: 510(k) (Traditional)
- Applicant: Smith & Nephew Richards, Inc.
- Decided: May 6, 1994 after 350 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.
246 later devices descend from it; 9 cite it directly.
0 of 247 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
- K993082: Exactech Acumatch Integrated Hip System a-Series Porous Coated Acetabular Component (1999), 161 descendants of its own
- K041906: Exactech 12/14 Total Hip System (2004), 145 descendants of its own
- K061253: Reflection 3 Acetabular System (2006), 120 descendants of its own
- K070756: Smith and Nephew Reflection 3 Acetabular System (2007), 91 descendants of its own
- K042842: Novation 12/14 Press-Fit Femoral Stem (2004), 64 descendants of its own

Source page: https://510kreport.com/device/K932755
Methodology: https://510kreport.com/methodology