# K241426: GPS Advanced; 5 cc GPS Advanced Cannula

- Pathway: 510(k) (Traditional)
- Applicant: Prosidyan, Inc.
- Decided: Jul 10, 2024 after 51 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: 13 generations back to K013966 (2002). 31 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 33 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K201338: Allograft MIS Delivery System, Lifenet Health (2020) Summary page 5.

## Most influential descendants
- K251648: GPS Advanced; GPS Advanced Cannula (2025), 0 descendants of its own

## Indications for use
GPS Advanced and GPS Advanced Cannula are intended for use to deliver FIBERGRAFT TM BG Putty GPS to a bone grafting site.

Source page: https://510kreport.com/device/K241426
Methodology: https://510kreport.com/methodology