# K071264: Synthes (Usa) 2.4/2.7 MM Locking Foot Module

- Pathway: 510(k) (Traditional)
- Applicant: Synthes (Usa)
- Decided: Jul 9, 2007 after 66 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.
299 later devices descend from it; 11 cite it directly.
0 of 300 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 (USA) LCP Modular Foot Plates: named in the summary without a submission number

## Most influential descendants
- K100776: Synthes 2.4 MM/2.7 MM Variable Angle LCP Forefoot/Midfoot System (2010), 228 descendants of its own
- K112583: Synthes Cortical Screws (2011), 118 descendants of its own
- K120070: Synthes Variable Angle LCP Elbow System (2012), 76 descendants of its own
- K110670: VLP Foot Talus Plates, VLP Percutaneous Calcaneus Plates and Misc VLP Bone Screws, Peri-Loc Ankle Fusion Plates (2011), 69 descendants of its own
- K121425: Ortholoc 3DI Ankle Fusion Plating System (2012), 53 descendants of its own

## Indications for use
The Synthes 2.4/2.7 mm Locking Foot Module is intended for fixation of fractures, osteotomies, nonunions, replantations, and fusions of small bones and small bone fragments, including the foot and ankle, particularly in osteopenic bone.

Source page: https://510kreport.com/device/K071264
Methodology: https://510kreport.com/methodology