Evo® sEEG System
Summary
Neuroone Medical Technologies Corp. received 510(k) clearance for Evo® sEEG System, a GZL device. Cleared on 2022-10-20.
Details
Source
510(k) Clearance
External ID
K222404
Action Date
2022-10-20
Status
Traditional
Category
device
Product Code
GZL
Product Description
Evo® sEEG System. Product code: GZL.
Context & Analysis
A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 403 device clearances issued this month. Neuroone Medical Technologies Corp. has received 4 total clearances in our database.
Neuroone Medical Technologies Corp. has 4 FDA actions in our database, including 4 clearances.
Frequently Asked Questions
What does 510(k) clearance mean?
A 510(k) is an FDA premarket submission demonstrating that a device is substantially equivalent to a legally marketed device. It does NOT mean FDA approval — it means the device is cleared for marketing because it's similar enough to an existing cleared device. Most medical devices reach market via 510(k) rather than full PMA approval.
How often does Neuroone Medical Technologies Corp. have FDA actions?
Neuroone Medical Technologies Corp. has 4 FDA actions in our database, including 0 recalls and 4 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K222404" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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