External CSF Drainage Ventricular Catheters, External CSF Drainage Lumbar Catheters
Summary
Sophysa received 510(k) clearance for External CSF Drainage Ventricular Catheters, External CSF Drainage Lumbar Catheters, a JXG device. Cleared on 2025-06-20.
Details
Source
510(k) Clearance
External ID
K242974
Action Date
2025-06-20
Status
Traditional
Category
device
Product Code
JXG
Product Description
External CSF Drainage Ventricular Catheters, External CSF Drainage Lumbar Catheters. Product code: JXG.
Company
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. Sophysa has received 4 total clearances in our database.
Sophysa has 5 FDA actions in our database, including 1 recall and 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 Sophysa have FDA actions?
Sophysa has 5 FDA actions in our database, including 1 recall and 4 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K242974" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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