# K150675: Dorsal Spanning Plate

- Pathway: 510(k) (Traditional)
- Applicant: Skeletal Dynamics, LLC
- Decided: May 12, 2015 after 57 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: 3 generations back to K000684 (2000). 16 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 18 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K093761: Optilock VL (Variable Angle Locking) Distal Radius Plating System, Biomet Trauma (Aka Ebi, Lp) (2010) Summary page 4.

## Most influential descendants
- K212601: DRPx Locking Distal Radius Plate System (2022), 0 descendants of its own

## Indications for use
The Skeletal Dynamics Dorsal Spanning Plate is intended for fixation of fractures involving the distal radius and for wrist arthrodesis.

Source page: https://510kreport.com/device/K150675
Methodology: https://510kreport.com/methodology