# K073076: Hoffmann Light System

- Pathway: 510(k) (Traditional)
- Applicant: Howmedica Osteonics Corp.
- Decided: Feb 15, 2008 after 107 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
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Hoffmann II External Fixation System: named in the summary without a submission number

## Most influential descendants
- K092834: Hoffman Xpress Line Extension (2009), 0 descendants of its own

## Indications for use
* Bone fracture fixation; * Osteotomy; * Arthodesis; * Correction of deformity; * Revision procedures where other treatments or devices have been unsuccessful; * Bone reconstruction procedures.

Source page: https://510kreport.com/device/K073076
Methodology: https://510kreport.com/methodology