510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K221629Substantially Equivalent

Tri-Staple™ 2.0 Black Circular Reloads (for use with Signia™ Circular Adapters)

Medtronic, Inc., North Haven CT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K221629 is the FDA 510(k) clearance record for Tri-Staple™ 2.0 Black Circular Reloads (for use with Signia™ Circular Adapters), a class II device, cleared for Covidien on under FDA product code GAG (Stapler, Surgical). FDA's definition for product code GAG reads: "A surgical stapler for internal use is a specialized prescription device used to deliver compatible staples to internal tissues during surgery for resection, transection, and creating anastomoses". FDA records list 1,525 510(k) clearances for Medtronic, Inc., from to . As of , FDA records show no recalls naming K221629.

Clearance record

Decision date
Received
(261 days to decision)
Product code
GAG Stapler, Surgical
Regulation
21 CFR 878.4740
Device class
Class II
Review panel
General Hospital
Applicant
Covidien 60 Middletown Ave., North Haven CT
510(k) summary
Summary PDF
Third party review
No

Clearances, product code GAG

Trailing 12 months
1 clearance under product code GAG in the twelve months to October 2026, July 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code GAG, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20261
August 20260
September 20260
October 20260