# K990212: Lockjaw 15 Minute Intermaxillary Fixation System,Model LJ100-00

- Pathway: 510(k) (Traditional)
- Applicant: Doctor'S Research Group, Inc.
- Decided: Sep 14, 1999 after 235 days
- Product code: DYX (Lock, Wire, And Ligature, Intraoral)
- Device class: 2
- Regulation: 21 CFR 872.4600
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The DRG LockJaw™ 15 Minute Intermaxillary Fixation System is intended for secondary intermaxillary fixation in the treatment of maxillary and mandibular fractures, in elective orthognathic surgery and in the stabilization of dental and dentoalveolar injuries.

Source page: https://510kreport.com/device/K990212
Methodology: https://510kreport.com/methodology