# K133437: 1ST MTP Plate

- Pathway: 510(k) (Special)
- Applicant: Osteomed
- Decided: Dec 2, 2013 after 25 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: 4 generations back to K981372 (1998). 7 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K131445: Osteomed Extremilock Foot Plating System, Osteomed LP (2013) Summary page 1.

## Most influential descendants
- K143365: Eminent Foot Plate System (2015), 1 descendant of its own
- K152548: AXI+LINE Proximal Bunion Correction System (2015), 0 descendants of its own

## Indications for use
The OsteoMed ExtremiLaCK Foot Plating System is indicated for use in trauma, general surgery, and reconstructive procedures of the root ankle or other bones appropriate for the size of the device. The OsteoMed ExtrendLOCK Foot Plating System implants are intended for single use only.

Source page: https://510kreport.com/device/K133437
Methodology: https://510kreport.com/methodology