# K072095: Synthes (Usa) Pediatric LCP Hip Plate System Modifications

- Pathway: 510(k) (Traditional)
- Applicant: Synthes (Usa)
- Decided: Sep 27, 2007 after 58 days
- Product code: JDS (Nail, 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.
13 later devices descend from it; 3 cite it directly.
0 of 14 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 Pediatric LCP Hip Plate System: named in the summary without a submission number
- (no number) Synthes Angled Blade Plates: named in the summary without a submission number

## Most influential descendants
- K111086: Orthopediatrics Fracture and Osteotomy Bone Plate System (2011), 7 descendants of its own
- K112085: Synthes LCP Pediatric Plate Systems (2011), 4 descendants of its own
- K192181: PRECICE Plating System (2019), 2 descendants of its own
- K200246: JPS JuniOrtho Plating System (2020), 1 descendant of its own
- K162307: OrthoPediatrics Locking Proximal Femur System Cortical Screws (2016), 1 descendant of its own

## Indications for use
The Synthes (USA) Pediatric LCP Hip Plate System is intended for fixation of fractures and osteotomies of the proximal femur in children, adolescents, and small statured adults. Specific indications include: • intertrochanteric rotational and/or varus osteotomies • femoral neck and/or pertrochanteric fractures • intertrochanteric valgus osteotomies and/or rotational osteotomies

Source page: https://510kreport.com/device/K072095
Methodology: https://510kreport.com/methodology