# K011032: Smartjet Bone Graft Liquid Applicator (Spray Tip), Model SK/S, Smartjet Bone Graft Liquid Applicator (Dual Lumen Cannula

- Pathway: 510(k) (Traditional)
- Applicant: Harvest Technologies, Corp.
- Decided: Jul 3, 2001 after 89 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; 3 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
- K021071: PCCS Graft Delivery System (2002), 49 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/K011032
Methodology: https://510kreport.com/methodology