510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K082640Substantially Equivalent

Virtue Ventral Urethral Elevation Sling System

MEDLINE INDUSTRIES, LP - Northfield, Minneapolis MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K082640 is the FDA 510(k) clearance record for VIRTUE VENTRAL URETHRAL ELEVATION SLING SYSTEM, a class II device, cleared for Coloplast Manufacturing Us, LLC on under FDA product code OTM (Mesh, Surgical, For Stress Urinary Incontinence, Male). FDA's definition for product code OTM reads: "surgical treatment of male stress urinary incontinence post-prostatectomy". FDA records list 414 510(k) clearances for MEDLINE INDUSTRIES, LP - Northfield, from to . As of , FDA records show no recalls naming K082640.

Clearance record

Decision date
Received
(37 days to decision)
Product code
OTM Mesh, Surgical, For Stress Urinary Incontinence, Male
Regulation
21 CFR 878.3300
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Coloplast Manufacturing Us, LLC 1499 W. River Rd. N., Minneapolis MN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code OTM

Trailing 12 months

FDA records hold no clearances under product code OTM in the trailing twelve months.

FDA records show no clearances under product code OTM in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code OTM, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260