# K052062: Alliance Medical Corporation Reprocessed External Fixation Devices

- Pathway: 510(k) (Special)
- Applicant: Alliance Medical Corp.
- Decided: Aug 25, 2005 after 27 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: 2 generations back to K802722 (1980). 4 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K012648: Reprocessed Howmedica External Fixation Devices, Alliance Medical Corp. (2002) Summary page 1.

## Most influential descendants
- K153415: Reprocessed Stryker External Fixation Devices (2016), 0 descendants of its own

## Indications for use
Reprocessed external fixation devices are indicated for use in patients requiring external skeletal fixation and treatment of fractures, osteotomy, arthrodesis, correction of deformities, fracture revision, bone reconstruction procedures, limb lengthening, correction of bony or soft tissue deformities and segmental bony or soft tissue defects.

Source page: https://510kreport.com/device/K052062
Methodology: https://510kreport.com/methodology