510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K200320Substantially Equivalent

Mirus Circular Stapler, Mirus Linear Cutter and Reload, Mirus Hemorrhoidal Circular Stapler, Mirus Linear Stapler and Reload

M/s. Meril Endo Surgery Private Limited., Chala, Vapi, IN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K200320 is the FDA 510(k) clearance record for Mirus Circular Stapler, Mirus Linear Cutter and Reload, Mirus Hemorrhoidal Circular Stapler, Mirus Linear Stapler and Reload, a class II device, cleared for M/s. Meril Endo Surgery Private Limited. on under FDA product code GDW (Staple, Implantable). FDA records list 12 510(k) clearances for M/s. Meril Endo Surgery Private Limited., from to . As of , FDA records show no recalls naming K200320.

Clearance record

Decision date
Received
(364 days to decision)
Product code
GDW Staple, Implantable
Regulation
21 CFR 878.4750
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
M/s. Meril Endo Surgery Private Limited. Third Floor, E1-E3, Meril Park, Survey # 135/2/B & 174/2,, Chala, Vapi, IN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code GDW

Trailing 12 months
4 clearances under product code GDW in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code GDW, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20260
March 20260
April 20261
May 20261
June 20260
July 20260
August 20260
September 20261
October 20260