# K240530: DynaNail Mini Tapered Hybrid

- Pathway: 510(k) (Special)
- Applicant: MedShape, Inc.
- Decided: Mar 21, 2024 after 27 days
- Product code: HWC (Screw, Fixation, Bone)
- Device class: 2
- Regulation: 21 CFR 888.3040
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 13 generations back to K962616 (1996). 81 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 84 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K203381: Dynanail Mini Hybrid, MedShape, Inc. (2021) Summary page 4.

## Most influential descendants
- K254110: DynaNail Mini; DynaNail Hybrid; DynaNail Helix; DynaClip; DynaClip Forte; DynaClip Delta; DynaClip Quattro (2026), 1 descendant of its own
- K260995: DynaNail Helix® Fixation System (2026), 0 descendants of its own

## Indications for use
The DynaNail Mini Tapered Hybrid is indicated for fracture fixation, osteotomies, reconstruction procedures, non-unions, and fusions of large bones in the foot and ankle.

Source page: https://510kreport.com/device/K240530
Methodology: https://510kreport.com/methodology