# K102688: Merete Locking Bone Plate System II

- Pathway: 510(k) (Traditional)
- Applicant: Merete Medical GmbH
- Decided: Dec 3, 2010 after 77 days
- Product code: KTT (Appliance, Fixation, Nail/Blade/Plate Combination, Multiple 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
Longest line of descent: 7 generations back to K981372 (1998). 15 ancestors in all.
No later device cites it as a predicate yet.
0 of 16 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K090063: Merete Locking Bone Plate System, Merete Medical, Inc. (2009) Summary page 1.
- K050457: Merete Metafix Small Fragment Bone Plate System, Merete Medical GmbH (2005) Summary page 1.
- K063487: Merete BLP Small Fragment Locking Bone Plate, Merete Medical GmbH (2007) Summary page 1.
- K081513: Merete 3.0 and 3.5 MM Locking Screws, Merete Medical GmbH (2008) Summary page 1.
- K061808: Darco Locking Bone Plate System, Darco International, Inc. (2006) Summary page 1.

## Indications for use
The Merete Locking Bone Plate System can be used for adult and pediatric patients. Indications for use include fixation of fresh fractures, revision procedures, joint fusion, and reconstruction of small bones of the hand, feet, wrist, ankles, fingers, and toes.

Source page: https://510kreport.com/device/K102688
Methodology: https://510kreport.com/methodology