# K993465: Depuy Ace Calcaneal Peri-Articular Plate

- Pathway: 510(k) (Traditional)
- Applicant: Depuy, Inc.
- Decided: Jan 11, 2000 after 90 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
Longest line of descent: 1 generation back to K915818 (1992). 1 ancestor in all.
42 later devices descend from it; 3 cite it directly.
0 of 44 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K915818: Synthes (R) Titanium Small Reconstruction Plate, Synthes (Usa) (1992) Summary page 2.
- (no number) DePuy ACE Calcaneal Plates: named in the summary without a submission number

## Most influential descendants
- K051642: FR.O.H. Calcaneus Repair System (2005), 28 descendants of its own
- K060156: Straight Plate with Angular Stability & Screw System (2006), 27 descendants of its own
- K041786: Calcamea Plate (2004), 13 descendants of its own
- K090582: Calcaneal Fracture Plate System (2009), 12 descendants of its own
- K132898: A.L.P.S. Calcaneal Plating System (2013), 11 descendants of its own

## Indications for use
The DePuy ACE Calcaneal Peri-Articular Plates are designed to assist the surgeon in the management of: Intra-articular fractures of the calcaneus Extra-articular fractures of the calcaneus

Source page: https://510kreport.com/device/K993465
Methodology: https://510kreport.com/methodology