# K072651: Cryospray Ablation System, Model CC2-Nam

- Pathway: 510(k) (Abbreviated)
- Applicant: CSA Medical, Inc.
- Decided: Dec 7, 2007 after 79 days
- Product code: GEH (Unit, Cryosurgical, Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4350
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K840536 (1984). 9 ancestors in all.
No later device cites it as a predicate yet.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K060555: Spraygenix Cryo Ablation System, Crymed Technologies, Inc. (2006) Summary page 1.
- K070893: Cryospray Ablation System, Model CU 8407020500, CSA Medical, Inc. (2007) Summary page 1.
- K040809: Crymed Cryo-Ablator, Crymed Technologies, Inc. (2004) Summary page 1.

## Indications for use
The CryoSpray AblationTM System is intended to be used as a cryosurgical tool for destruction of unwanted tissue in the field of general surgery, specifically for endoscopic applications.

Source page: https://510kreport.com/device/K072651
Methodology: https://510kreport.com/methodology