# K181781: DynaClipTM Bone Staple

- Pathway: 510(k) (Traditional)
- Applicant: MedShape, Inc.
- Decided: Nov 5, 2018 after 125 days
- Product code: JDR (Staple, 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 K902307 (1990). 5 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K124045: Fuseforce Implant System, Solana Surgical, LLC (2013) 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 MedShape DynaClip™ Bone Staple is intended to be used for fracture and osteotomy fixation and joint arthrodesis of the hand and foot.

Source page: https://510kreport.com/device/K181781
Methodology: https://510kreport.com/methodology