UNITY Sacroiliac Joint Fixation System
Summary
Dio Medical Corporation received 510(k) clearance for UNITY Sacroiliac Joint Fixation System, a OUR device. Cleared on 2022-10-13.
Details
Source
510(k) Clearance
External ID
K222448
Action Date
2022-10-13
Status
Traditional
Category
device
Product Code
OUR
Product Description
UNITY Sacroiliac Joint Fixation System. Product code: OUR.
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. Dio Medical Corporation has received 4 total clearances in our database.
Dio Medical Corporation 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 Dio Medical Corporation have FDA actions?
Dio Medical Corporation 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 "K222448" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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