510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K063079Substantially Equivalent

I-Stop Trans Obturator Male Sling

CL MEDICAL Inc., Sainte Foy Les Lyon, FR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K063079 is the FDA 510(k) clearance record for I-STOP TRANS OBTURATOR MALE SLING, a class II device, cleared for Cl Medical 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 2 510(k) clearances for Cl Medical, from to . As of , FDA records show no recalls naming K063079.

Clearance record

Decision date
Received
(28 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
Cl Medical 28 Ave. General De Gaulle, Sainte Foy Les Lyon, FR
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