EUROSCREW NG; EUROSCREW TCP NG
Summary
Teknimed received 510(k) clearance for EUROSCREW NG; EUROSCREW TCP NG, a MAI device. Cleared on 2023-05-12.
Details
Source
510(k) Clearance
External ID
K230394
Action Date
2023-05-12
Status
Traditional
Category
device
Product Code
MAI
Product Description
EUROSCREW NG; EUROSCREW TCP NG. Product code: MAI.
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.
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 Teknimed have FDA actions?
This is the only FDA action we have on record for Teknimed in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K230394" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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