# K062920: Orthofix Titanium Humeral Plating System LSP

- Pathway: 510(k) (Traditional)
- Applicant: Orthofix Srl
- Decided: Nov 13, 2006 after 46 days
- Product code: KTW (Appliance, Fixation, Nail/Blade/Plate Combination, Single 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.
1 later device descends from it; 1 cites it directly.
0 of 2 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 no predicate by number.

## Most influential descendants
- K122541: Orthofix Contours Proimal Humeral Plate (PHP) (2012), 0 descendants of its own

## Indications for use
The Orthofix Titanium Humeral Plating System is intended for fractures, osteotomies and non-unions of the proximal humerus, particularly in osteopenic bone.

Source page: https://510kreport.com/device/K062920
Methodology: https://510kreport.com/methodology