510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K211178Substantially Equivalent

DURAMESH Mesh Suture

Msi, Chicago IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K211178 is the FDA 510(k) clearance record for DURAMESH Mesh Suture, a class II device, cleared for Msi on under FDA product code GAW (Suture, Nonabsorbable, Synthetic, Polypropylene). FDA records list one 510(k) clearance for Msi. As of , FDA records show no recalls naming K211178.

Clearance record

Decision date
Received
(500 days to decision)
Product code
GAW Suture, Nonabsorbable, Synthetic, Polypropylene
Regulation
21 CFR 878.5010
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Msi One Magnificent Mile, Chicago IL
510(k) summary
Summary PDF
Third party review
No

Clearances, product code GAW

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