# K010321: Modular Foot System - 2.7 MM Module

- Pathway: 510(k) (Traditional)
- Applicant: Synthes (Usa)
- Decided: May 2, 2001 after 89 days
- Product code: KTW (Appliance, Fixation, Nail/Blade/Plate Combination, Single 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
No predicates in its family tree.
200 later devices descend from it; 9 cite it directly.
0 of 201 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K112583: Synthes Cortical Screws (2011), 118 descendants of its own
- K060473: TTC Plate (2006), 76 descendants of its own
- K073375: Newdeal Tibiaxys System (2008), 73 descendants of its own
- K110670: VLP Foot Talus Plates, VLP Percutaneous Calcaneus Plates and Misc VLP Bone Screws, Peri-Loc Ankle Fusion Plates (2011), 69 descendants of its own
- K100176: Ascension Ankle Fusion Plate System (2010), 56 descendants of its own

Source page: https://510kreport.com/device/K010321
Methodology: https://510kreport.com/methodology