# K010320: Modification to Symphony Graft Delivery System

- Pathway: 510(k) (Special)
- Applicant: Depuyacromed
- Decided: Mar 1, 2001 after 27 days
- Product code: LYC (Bone Grafting Material, Synthetic)
- Device class: 2
- Regulation: 21 CFR 872.3930
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
53 later devices descend from it; 2 cite it directly.
0 of 54 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
- K022246: Modification to Symphony Graft Delivery System (2002), 51 descendants of its own
- K072330: Controlled Delivery for Osteoplasty (Cdo System) and Graft Preparation System (2007), 47 descendants of its own
- K100754: Graft Delivery System Model SA-6115 (2010), 45 descendants of its own
- K111632: Infill Graft Delivery System (2011), 41 descendants of its own
- K121476: Infill Graft Delivery System (2012), 40 descendants of its own

Source page: https://510kreport.com/device/K010320
Methodology: https://510kreport.com/methodology