ARIX Ankle System
Summary
Jeil Medical Corporation received 510(k) clearance for ARIX Ankle System, a HRS device. Cleared on 2023-07-17.
Details
Source
510(k) Clearance
External ID
K231441
Action Date
2023-07-17
Status
Traditional
Category
device
Product Code
HRS
Product Description
ARIX Ankle System. Product code: HRS.
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. Jeil Medical Corporation has received 16 total clearances in our database.
Jeil Medical Corporation has 16 FDA actions in our database, including 16 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 Jeil Medical Corporation have FDA actions?
Jeil Medical Corporation has 16 FDA actions in our database, including 0 recalls and 16 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K231441" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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