# K180937: Graftgun Universal Graft Delivery System

- Pathway: 510(k) (Special)
- Applicant: SurGenTec, LLC
- Decided: May 10, 2018 after 30 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: 11 generations back to K013966 (2002). 29 ancestors in all.
6 later devices descend from it; 4 cite it directly.
0 of 36 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K170675: Graftgun Universal Graft Delivery System, SurGenTec, LLC (2017) Summary page 4.

## Most influential descendants
- K201338: Allograft MIS Delivery System (2020), 2 descendants of its own
- K243580: GraftGun Universal Graft Delivery System (GDS) (2025), 1 descendant of its own
- K241426: GPS Advanced; 5 cc GPS Advanced Cannula (2024), 1 descendant of its own
- K262581: GraftGun Universal Graft Delivery System (GDS®) (2026), 0 descendants of its own
- K251648: GPS Advanced; GPS Advanced Cannula (2025), 0 descendants of its own

## Indications for use
The Graftgun Universal Graft Delivery System is intended to be used for the delivery of hydrated allograft, autograft, or synthetic bone graft material to an orthopedic surgical site.

Source page: https://510kreport.com/device/K180937
Methodology: https://510kreport.com/methodology