# K020252: Smartjet Grafting Liquid Applicator, Models SK/S & LK/2

- Pathway: 510(k) (Traditional)
- Applicant: Harvest Technologies, Corp.
- Decided: Apr 5, 2002 after 71 days
- Product code: FMF (Syringe, Piston)
- Device class: 2
- Regulation: 21 CFR 880.5860
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K011032 (2001). 1 ancestor in all.
2 later devices descend from it; 2 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K011032: Smartjet Bone Graft Liquid Applicator (Spray Tip), Model SK/S, Smartjet Bone Graft Liquid Applicator (Dual Lumen Cannula, Harvest Technologies, Corp. (2001) Summary page 1.

## Most influential descendants
- K091722: Coaxial Applicator System (2010), 0 descendants of its own
- K041830: Magellan Ratio Dispenser Kit (2004), 0 descendants of its own

## Indications for use
The SmartJet Grafting Liquid Applicator is intended for the application of fluids, as deemed necessary by the surgeon’s determination of the clinical use requirements, to facilitate the preparation of soft tissue autograft or allograft material prior to the application of the graft material to a repair site.

Source page: https://510kreport.com/device/K020252
Methodology: https://510kreport.com/methodology