# K120645: Pro-Toe (TM) VO Hamertoe Implant System-Line Sddition

- Pathway: 510(k) (Traditional)
- Applicant: Wrightmedicaltechnologyinc
- Decided: Apr 24, 2012 after 53 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: 3 generations back to K960385 (1996). 4 ancestors in all.
61 later devices descend from it; 7 cite it directly.
0 of 66 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K101165: Pro-Toe VO Hammertow Implant System, Wrightmedicaltechnologyinc (2010)
- K022599: Newdeal K Wire, New Deal, S.A. (2002) Summary page 1.

## Most influential descendants
- K133636: Extremity Medical Hammertoe Device (2014), 31 descendants of its own
- K132895: WMT Implantable K-Wire (2013), 27 descendants of its own
- K140148: Pro-Toe Hammertoe Fixation System (2014), 20 descendants of its own
- K141857: CrossTie Intraosseous Fixation System (2015), 16 descendants of its own
- K151270: CrossTIE Intraosseous Fixation System (2015), 15 descendants of its own

## Indications for use
The Pro-ToeTM VO. Hammertoe Implant System is indicated for the fixation of osteotomies and reconstruction of the lesser toes following correction procedures for hammertoe, claw toe, and mallet toe.

Source page: https://510kreport.com/device/K120645
Methodology: https://510kreport.com/methodology