# K132895: WMT Implantable K-Wire

- Pathway: 510(k) (Traditional)
- Applicant: Wrightmedicaltechnologyinc
- Decided: Oct 23, 2013 after 37 days
- Product code: HTY (Pin, Fixation, Smooth)
- 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: 4 generations back to K960385 (1996). 5 ancestors in all.
27 later devices descend from it; 9 cite it directly.
0 of 33 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)
- K120645: Pro-Toe (TM) VO Hamertoe Implant System-Line Sddition, Wrightmedicaltechnologyinc (2012) Summary page 1.
- K022599: Newdeal K Wire, New Deal, S.A. (2002) Summary page 1.

## Most influential descendants
- K140148: Pro-Toe Hammertoe Fixation System (2014), 20 descendants of its own
- K142585: PhaLinx Hammertoe System (2014), 9 descendants of its own
- K150252: PHALINX Hammertoe System (2015), 6 descendants of its own
- K151838: PRO-TOE Hammertoe Fixation System (2015), 4 descendants of its own
- K200840: DuoHex CH Cannulated Hammertoe System (2020), 3 descendants of its own

## Indications for use
The WMT Implantable K-Wires are indicated for use in fixation of bone fractures, for bone reconstructions, and as guide pins for insertion of other implants. Additionally, WMT Implantable K-Wires are indicated for the fixation of osteotomies and reconstruction of the lesser toes following correction procedures for hammertoe, claw toe, mallet toe, and metatarsophalangeal joint instability.

Source page: https://510kreport.com/device/K132895
Methodology: https://510kreport.com/methodology