# K062564: Synthes LCP Distal Femur Plates

- Pathway: 510(k) (Traditional)
- Applicant: Synthes (Usa)
- Decided: Oct 19, 2006 after 49 days
- Product code: HRS (Plate, Fixation, Bone)
- Device class: 2
- Regulation: 21 CFR 888.3030
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
150 later devices descend from it; 25 cite it directly.
0 of 151 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Synthes LCP Curved Condylar Plates: named in the summary without a submission number

## Most influential descendants
- K110354: 4.5MM VA-LCP Curved Condylar Plate System (2011), 62 descendants of its own
- K083286: Orthopediatrics Pediloc Locking Plate System (2009), 60 descendants of its own
- K120854: Synthes VA LCP Ankle Trauma System (2012), 44 descendants of its own
- K120689: Synthes 3.5 MM VA-LCP Proximal Tibia Plate System (2012), 28 descendants of its own
- K143385: Acumed Ankle Plating System (2015), 23 descendants of its own

## Indications for use
Synthes LCP Distal Femur Plates are intended for buttressing multifragmentary distal femur fractures including: supracondylar, intra-articular and extra-articular condylar, periprosthetic fractures and fractures in normal or osteopenic bone, nonunions and malunions, and osteotomies of the femur.

Source page: https://510kreport.com/device/K062564
Methodology: https://510kreport.com/methodology