510(k) K221006

GIA Stapler with Tri-Staple Technology by Covidien — Product Code GDW

K221006 is an FDA 510(k) premarket notification submitted by Covidien for the device "GIA Stapler with Tri-Staple Technology". The FDA issued a decision of Substantially Equivalent on April 29, 2022. The device falls under product code GDW (Staple, Implantable), a Class II device regulated under 21 CFR 878.4750. Covidien has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 29, 2022
Date Received
April 5, 2022
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Staple, Implantable
Device Class
Class II
Regulation Number
878.4750
Review Panel
SU
Submission Type