# K063509: Depuy Peak FX Hip Plate

- Pathway: 510(k) (Traditional)
- Applicant: DePuy Orthopaedics, Inc.
- Decided: Jan 4, 2007 after 45 days
- Product code: KTT (Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component)
- 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
Longest line of descent: 1 generation back to K813554 (1982). 1 ancestor in all.
35 later devices descend from it; 1 cites it directly.
0 of 37 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K813554: Ace/Kyle Captured Hip Screw, Ace Orthopedic Manufacturing Co. (1982) Summary page 1.

## Most influential descendants
- K090656: Intertan CHS Limited Collapse Set Screw (2009), 34 descendants of its own
- K123055: Smith & Nephew, Inc Screw and Plate System Instrumentation (2013), 33 descendants of its own
- K140814: Evos Mini-Fragment Plating System (2014), 32 descendants of its own
- K163361: ANTHEM™ Fracture System (2017), 14 descendants of its own
- K173166: ANTHEM Fracture System (2017), 11 descendants of its own

## Indications for use
The Peak Fx Hip Plate is indicated for the following fractures of the proximal femur: * Basilar neck fractures * Intertrochanteric fractures * Subtrochanteric fractures The Peak Fx Hip Plate is indicated for stable and unstable fractures in which a stable medial buttress can be reconstructed.

Source page: https://510kreport.com/device/K063509
Methodology: https://510kreport.com/methodology