# K010766: Synthes (Usa) Large Fragment Locking Compression Plate (LCP) System-T Plate

- Pathway: 510(k) (Traditional)
- Applicant: Synthes (Usa)
- Decided: Jun 12, 2001 after 90 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
No predicates in its family tree.
24 later devices descend from it; 7 cite it directly.
0 of 25 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 T Plates: named in the summary without a submission number

## Most influential descendants
- K130108: Double Engine Bone Plate and Screw Systems (2013), 9 descendants of its own
- K180310: DePuy Synthes Trauma Orthopedic Plates and Screws (2018), 4 descendants of its own
- K042237: Ebi Periarticular Plating System (2004), 3 descendants of its own
- K092078: Optilock Periarticular Plating (2009), 2 descendants of its own
- K243995: Arthrex Humeral Plating System and Cerclage Button (2025), 1 descendant of its own

## Indications for use
Intended to buttress metaphyseal fractures of the proximal humerus, medial tibial plateau and distal tibia. Also for use in the fixation of osteopenic bone and fixation of non-unions and malunions.

Source page: https://510kreport.com/device/K010766
Methodology: https://510kreport.com/methodology