EEACircular Stapler with Tri-Staple Technology and OrVil Transoral Circular Stapler Anvil
Summary
Covidien received 510(k) clearance for EEACircular Stapler with Tri-Staple Technology and OrVil Transoral Circular Stapler Anvil, a GAG device. Cleared on 2023-08-16.
Details
Source
510(k) Clearance
External ID
K232126
Action Date
2023-08-16
Status
Special
Category
device
Product Code
GAG
Product Description
EEACircular Stapler with Tri-Staple Technology and OrVil Transoral Circular Stapler Anvil. Product code: GAG.
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. Covidien has received 16 total clearances in our database.
Covidien has 33 FDA actions in our database, including 17 recalls and 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 Covidien have FDA actions?
Covidien has 33 FDA actions in our database, including 17 recalls and 16 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K232126" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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