# K031959: Stryker Plating System Periarticular Plates

- Pathway: 510(k) (Special)
- Applicant: Howmedica Osteonics Corp.
- Decided: Jul 25, 2003 after 30 days
- Product code: LXT (Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite)
- 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.
No later device cites it as a predicate yet.
0 of 1 device 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) SPS Small Fragment Set: named in the summary without a submission number
- (no number) SPS Basic Fragment Set: named in the summary without a submission number

## Indications for use
The 3.5mm and 4.5mm Periarticular Plate components are intended for use in long bone fracture fixation. The 3.5mm and 4.5mm proximal tibial Periarticular Plates are indicated for fixation of long bone fractures, including, but not limited to, fractures of the tibia. The 4.5mm distal femur Periarticular Plates are indicated for fixation of long bone fractures, including, but not limited to, fractures of the femur.

Source page: https://510kreport.com/device/K031959
Methodology: https://510kreport.com/methodology