# K152145: OsteoMed ExtremiLOCK Wrist Plating System

- Pathway: 510(k) (Traditional)
- Applicant: Osteomed
- Decided: Dec 21, 2015 after 140 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: 8 generations back to K962616 (1996). 58 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 60 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K120015: Osteomed Wrist Plating System, Osteomed LP (2012) Summary page 4.
- K083694: Synthes (Usa) 2.4 MM VA-LCP Two Column Volar Distal Radius Plates, Synthes (Usa) (2009) Summary page 4.

## Most influential descendants
- K161041: OsteoMed ExtremiLOCK Wrist Plating System (2016), 0 descendants of its own

## Indications for use
OsteoMed ExtremiLOCK Wrist Plating System is indicated for fracture fixation, fusion and osteotomies of wrist and other bones appropriate for the size of the device. It is intended for use in trauma, general surgery, and reconstructive procedures. OsteoMed ExtremiLOCK Wrist Plating System implants are intended for single use only.

Source page: https://510kreport.com/device/K152145
Methodology: https://510kreport.com/methodology