# K120978: Osteobridge Ika Knee Arthodesis Nail with Collar

- Pathway: 510(k) (Special)
- Applicant: Merete Medical GmbH
- Decided: May 2, 2012 after 30 days
- Product code: HSB (Rod, Fixation, Intramedullary And Accessories)
- Device class: 2
- Regulation: 21 CFR 888.3020
- 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
Intramedullary knee arthrodesis Indications include: 1. Irretrievably failed total knee arthroplasty 2. Limb salvage 3. Oncology surgery 4. Any other condition where there is little soft tissue or bony tissue available for support and arthrodesis is the treatment of choice The intramedullary. rods can be fixed with interlocking screws without or with bone cement.

Source page: https://510kreport.com/device/K120978
Methodology: https://510kreport.com/methodology