SeedNet System and SeedNetGold System
by Galil Medical Ltd 510(k)
Active
510(k) K031117
Overview
The SeedNet System and SeedNetGold System are cryosurgical units and accessories designed for the cryogenic destruction of tissue during surgical procedures. These systems function as cryosurgical tools used in fields including general surgery, dermatology, neurology, and thoracic surgery.
The devices are authorized under FDA 510(k) clearance K031117. They are intended for use by medical professionals in clinical settings for precise tissue destruction.
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK031117 | Date23 May 2003 | StatusActive |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — FDA 510(k) Active
Recalls
No FDA recalls on record, checked 22 Oct 2026.
Specification
- 510(k) Number
- FDA Product Code
- GEH
- FDA applicant
- Galil Medical , Ltd.
- Device Class
- Class II
- Regulation
- 21 CFR Part 878.4350
- Advisory Committee
- General, Plastic Surgery
- FDA Decision
- SESE Substantially Equivalent
Other devices from Galil Medical Ltd
Questions
What are the SeedNet and SeedNetGold systems used for?
These systems are cryosurgical tools intended for the cryogenic destruction of tissue. They are designed for use by medical professionals in clinical settings across various fields, including general surgery, dermatology, neurology, and thoracic surgery.
What is the regulatory status of these devices?
The SeedNet System and SeedNetGold System are authorized under FDA 510(k) clearance K031117. This indicates the devices have been reviewed and cleared for clinical use.
Who manufactures the SeedNet cryosurgical units?
The SeedNet and SeedNetGold systems are manufactured by Galil Medical Ltd., located in Yokneam, Israel.