# K133235: Threaded Peek K-Wire

- Pathway: 510(k) (Traditional)
- Applicant: Mtp Solutions, LLC
- Decided: Apr 7, 2014 after 168 days
- Product code: MBI (Fastener, Fixation, Nondegradable, Soft Tissue)
- 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: 7 generations back to K961555 (1996). 14 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 17 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K101679: Arthrex Pushlock Anchors, Arthrex, Inc. (2010) Summary page 2.
- K082810: Arthrex Bio-Composite Suture Anchors: Arthrex Bio-Composite Pushlock, Bio-Composite Tak and Bio-Composite Corkscrew, Arthrex, Inc. (2009) Summary page 2.
- K071177: Arthrex Bio- Composite Suture Anchors: Bio-Composite Pushlock, Bio-Composite Tak, Bio-Composite Corkscrew, Arthrex, Inc. (2007) Summary page 2.
- K063479: Arthrex Pushlock, Arthrex, Inc. (2006) Summary page 2.
- K061863: Arthrex Corkscrew Suture Anchor, Tak, and Pushlock Family, Arthrex, Inc. (2006) Summary page 2.
- K051219: Pushlock, Arthrex, Inc. (2005) Summary page 2.

## Most influential descendants
- K160118: STROPP (Single Tunnel Repair of Plantar Plate) (2016), 0 descendants of its own
- K151241: Synchro-Medical TIGER TRACK Screw System (2015), 0 descendants of its own

## Indications for use
The Threaded PEEK K-Wire is intended for use with suture in metatarsal ligament and tendon repairs.

Source page: https://510kreport.com/device/K133235
Methodology: https://510kreport.com/methodology