# K925447: Oti Orthopedic Wire System

- Pathway: 510(k) (Traditional)
- Applicant: Osteo Technology, Inc.
- Decided: Jun 29, 1993 after 244 days
- Product code: JDQ (Cerclage, Fixation)
- Device class: 2
- Regulation: 21 CFR 888.3010
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
9 later devices descend from it; 1 cites it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K110895: Ortho Solutions Trauma Implants for Osteosynthesis (2011), 8 descendants of its own
- K163489: OrthoSolutions 'System26' Bone Screws (2017), 3 descendants of its own
- K150889: Suture Wires and Wire Loops (2015), 2 descendants of its own
- K203773: BRM TOOL Screws (2022), 1 descendant of its own
- K151848: Cable-Ready® Cable Grip System: Cable-Ready Pin System, Cable-Ready Needle System (2016), 1 descendant of its own

Source page: https://510kreport.com/device/K925447
Methodology: https://510kreport.com/methodology