# K011218: Acumatch L-Series Cemented Femoral Stem, Model Size 1

- Pathway: 510(k) (Special)
- Applicant: Exactech, Inc.
- Decided: May 16, 2001 after 26 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.
4 later devices descend from it; 2 cite it directly.
0 of 5 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
- K052787: Acumatch 12/14 C-Series Cemented Femoral Stems (Size 1-6), Acumatch 12/14 L-Series Cemented Femoral Stems (Size 1-5) (2005), 2 descendants of its own
- K083392: Novation 12/14 Cemented Femoral Stems (2008), 1 descendant of its own
- K090764: Novation CFS Press-Fit and Cemented Stems (2009), 0 descendants of its own
- K012493: Acumatch C-Series Cemented Femoral Component, Model Size 0 (2001), 0 descendants of its own

Source page: https://510kreport.com/device/K011218
Methodology: https://510kreport.com/methodology