# K110271: Maestro Wrist Plating System

- Pathway: 510(k) (Traditional)
- Applicant: Biomet Manufacturing Corp
- Decided: Jul 22, 2011 after 172 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.
No later device cites it as a predicate yet.
0 of 17 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 1.
- K040908: Ebi Distal Radius Plating System, Ebi, L.P. (2004) Summary page 1.

## Indications for use
The Maestro® Wrist Plating System is indicated for fractures, fracture dislocations, osteotomies and non-unions of the distal radius and ulna.

Source page: https://510kreport.com/device/K110271
Methodology: https://510kreport.com/methodology