# K010551: Ebi Dynafix VS Osteotomy System

- Pathway: 510(k) (Traditional)
- Applicant: Ebi, L.P.
- Decided: May 17, 2001 after 80 days
- Product code: NDF (Plate, Fixation, Bone, Non-Spinal, Metallic)
- 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. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K021749: Ebi Dynafix VS Osteotomy System (2002), 0 descendants of its own

Source page: https://510kreport.com/device/K010551
Methodology: https://510kreport.com/methodology