# K092834: Hoffman Xpress Line Extension

- Pathway: 510(k) (Special)
- Applicant: Howmedica Osteonics Corp.
- Decided: Oct 8, 2009 after 23 days
- Product code: KTT (Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component)
- Device class: 2
- Regulation: 21 CFR 888.3030
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K073076 (2008). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K073076: Hoffmann Light System, Howmedica Osteonics Corp. (2008) Summary page 2.

## Indications for use
The Hoffmann Xpress Line Extension is intended for complete and temporary fracture fixation for long bones and pelvis fractures. Specific indications include: * Bone fracture fixation; * Osteotomny; * Arthodesis; * Correction of deformity; * Revision procedures where other treatments or devices have been unsuccessful; * Bone reconstruction procedures.

Source page: https://510kreport.com/device/K092834
Methodology: https://510kreport.com/methodology